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<h3>Job Description</h3>
Job Description
Drug Hunter™ (drughunter.com) is an essential knowledge platform for industry R&amp;D innovators turning molecules into medicines. The Drug Hunter research team distills the science behind emerging drugs and technologies into concise but scientifically rich, searchable reports. Drug Hunter subscribers include many of the world’s leading innovative biotechnology and pharmaceutical companies and top-tier investors.
The Industry Research Scientist will play a crucial role in building relationships with our members through product and feature demonstrations and trainings, facilitating events and workshops highlighting the power of the Drug Hunter platform, and creating and curating high-quality educational content for Drug Hunter’s audience of industry professionals. This role requires scientific expertise, a strong understanding of industry trends, and exceptional communication skills to distill complex information into engaging resources.
Key Responsibilities:
<ul>
<li>Conduct engaging demonstrations to technical audiences including PhD medicinal chemists, showcasing the capabilities of the Drug Hunter platform</li>
<li>Develop and deliver presentations tailored to Drug Hunter members and prospects working in small molecule drug discovery</li>
<li>Present highlights in small molecule drug discovery featuring content curated from Drug Hunter to inform and inspire audiences</li>
<li>Stay informed and report on the latest trends, breakthroughs, and developments in small molecule drug discovery within the pharmaceutical and biotechnology industries.</li>
<li>Synthesize information from multiple sources into concise, insightful educational content (e.g., reviews on scientific concepts, drug targets, modalities, and technologies).</li>
<li>Prepare educational articles and summaries based on webinars, interviews, and recordings on a regular basis.</li>
<li>Develop and review a variety of educational resources for Drug Hunter members, including cheat sheets, calculators, posters, and directories.</li>
<li>Create and review engaging social media posts to promote Drug Hunter articles, events, and webinars.</li>
<li>Prepare and review content for newsletters, ensuring relevance and value for different audience segments.</li>
<li>Collaborate cross-functionally with editorial, marketing, business development, sales, and product teams to develop presentations, webinars, demos, and articles.</li>
<li>Contribute to the production of video and audio content for educational and marketing purposes.</li>
<li>Attend and organize mixers, dinners, and other networking events</li>
<li>Other duties as required</li>
</ul>
Requirements
<ul>
<li>Ph.D. in chemistry, pharmacology, biochemistry, or a related scientific field.</li>
<li>3+ years of experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery.</li>
<li>Strong scientific writing, editing, and data synthesis skills.</li>
<li>Ability to independently research and distill complex scientific topics for a professional audience.</li>
<li>Digitally native, comfortable with social media, software, databases, literature search tools, and new technologies and platforms, and eager to apply new best practices to a growing organization</li>
<li>Proven ability to collaborate effectively across teams in a remote work environment.</li>
<li>Ability to work independently and collaboratively in an extremely fast-paced, dynamic environment and meet strict deadlines </li>
</ul>
Preferred Qualifications:
<ul>
<li>Familiarity with Drug Hunter's platform and tools</li>
<li>Established network within the pharmaceutical and biotechnology industries</li>
<li>Experience with scientific content creation and data analysis</li>
</ul>
Instructions To Apply:
Your application should include:
<ol>
<li>A resume or CV</li>
<li>A cover letter stating why you are excited about this opportunity</li>
<li>A draft for a social media post about a recent ground-breaking development in small molecule drug discovery illustrated with an image written independently by you </li>
</ol>
Applications are considered on a rolling basis.
Benefits
Why join Drug Hunter?
<ul>
<li>Be part of a dynamic and innovative team that is at the forefront of the pharmaceutical industry and scientific innovation</li>
<li>Contribute to a platform that influences drug discovery and development worldwide</li>
<li>Engage with leading experts and industry partners, expanding your professional network</li>
<li>Enjoy a flexible work environment with opportunities for growth and professional development</li>
</ul>
Drug Hunter provides industry-leading benefits, including the following:
<ul>
<li>Competitive salary, variable compensation, and equity</li>
<li>Broad range of medical, dental, vision, and life insurance plans for employees and their dependents, including generous coverage for a platinum PPO healthcare plan</li>
<li>Short-term disability and long-term disability insurance</li>
<li>Cancer and critical illness coverage</li>
<li>Up to 12 weeks paid parental leave (after 1 yr tenure) and childcare FSA plan</li>
<li>401(k) + employer match (3-5%)</li>
<li>Home office set up stipend for fully remote employees</li>
<li>Learning and development support</li>
<li>Generous and flexible vacation and leave policies</li>
</ul>

Industry Research Scientist

<h3>Job Description</h3>
Title: R&amp;D Scientist Lead
Compensation: $130000 plus bonus &amp; benefits, commensurate with experience. Ownership Program (Equity)
Location: Southwest of Boston (On-site)
 
Company Description: 
Our client is recognized as a leading manufacturer of protective materials for high reliability applications throughout the world. If you are looking for an incredibly stable company that continues to show outstanding expansion to new markets, then apply now. This is your chance to put your talents and experience to work for a company that offers excellent personal growth, great benefits and support. Take advantage of this amazing opportunity before someone else does.
 
Position Description:
The R&amp;D Group Lead will oversee a small team responsible for the development of liquid-applied coatings, pressure-sensitive tapes, and membranes for the Corrosion Protection &amp; Waterproofing business unit. This role manages New Product Development (NPD) projects, ensuring they meet performance criteria, timelines, and commercialization goals. The Group Lead will also play a key role in R&amp;D leadership, collaborating cross-functionally with Sales, Marketing, Operations, Quality, and Supply Chain to support innovation and business growth.
 
Responsibilities: 
<ul>
<li>Team Leadership &amp; Project Management</li>
<li>Lead, mentor, and develop the Corrosion Protection &amp; Waterproofing R&amp;D team.</li>
<li>Oversee new product development, scale-up, and field testing, ensuring alignment with business objectives.</li>
<li>Manage project timelines, adjusting priorities as needed to meet strict deadlines.</li>
<li>Support cross-functional collaboration in technology transfer, pilot plant trials, and commercialization efforts.</li>
<li>Technical Expertise &amp; Innovation</li>
<li>Apply expertise in polyurethane, epoxy, pressure-sensitive adhesives, and other coatings technologies.</li>
<li>Support the sourcing and qualification of new raw materials.</li>
<li>Work in close association with Sales, Marketing, Supply chain and Operations teams.</li>
<li>Identify and assess potential new product development opportunities with Marketing and Commercial teams.</li>
<li>Manufacturing &amp; Quality Support</li>
<li>Assist Operations and Quality teams across multiple manufacturing sites (travel: 10-25%).</li>
<li>Ensure adherence to ISO 9001 quality standards and participate in internal, external, and customer audits.</li>
<li>Promote and uphold safety standards at the Westwood R&amp;D site.</li>
<li>Strategic &amp; Cross-Functional Leadership</li>
<li>Participate in R&amp;D leadership initiatives to drive continuous improvement.</li>
<li>Track and report Key Performance Indicators (KPIs) and project updates to senior leadership.</li>
<li>Engage in cross-functional work teams within our client's business units.</li>
</ul>
 
Qualifications: 
<ul>
<li>Minimum 5 years of experience leading R&amp;D teams and manage product development projects.</li>
<li>Strong knowledge of coatings, adhesives, and regulatory standards.</li>
<li>Experience with Stage Gate processes and project management methodologies.</li>
<li>Excellent organizational, written, and verbal communication skills.</li>
<li>Willingness to travel (up to 25%) for manufacturing support and product trials.</li>
</ul>
 Education &amp; Certifications:
<ul>
<li>Master's or Ph.D. in Chemistry, Materials Science, Chemical Engineering, or equivalent industry experience.</li>
</ul>
 Benefits: 
<ul>
<li>Discretionary Bonus</li>
<li>Ownership Program (Equity)</li>
<li>401K</li>
<li>Medical / Dental / Vision</li>
</ul>
 Equal Opportunity Statement:
RCM is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
 
Pay Transparency:
RCM believes in transparency and fairness in compensation. We are committed to providing our employees with competitive salaries that reflect their skills, experience, and contributions to our organization. As part of our commitment to pay transparency, we want to provide you with as much information as possible about our compensation practices.
 
Disclaimer:
This job posting is intended to describe the general nature and the level of the work to be performed. It is not intended to include every job duty and responsibility specific to the position. RCM reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
 
About RCM:
RCM is a leading provider of Business, IT, and Engineering Services to over 1,000 clients in the commercial marketplace. RCM partners with clients to define, implement and manage a broad range of technologies across multiple platforms, systems, and networks. Our broad geographic presence ensures that a proven and reliable tactical and strategic capability is available and deployable virtually everywhere in North America.

Sr. R&D Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Cleanroom Assembler Job Description
Join our team as a Cleanroom Assembler, where you will contribute to producing superior medical product assemblies in a regulated environment. This role is ideal for individuals with a keen eye for detail, good attendance, and a willingness to learn.
Responsibilities
<ul>
<li>Assemble and package products with precision.</li>
<li>Complete paperwork for related assemblies and production activities.</li>
<li>Communicate discrepancies or potential issues as needed.</li>
<li>Utilize mechanical, electrical, and optical tools and equipment for quality inspections.</li>
<li>Ensure high-quality standards in assembly production.</li>
<li>Operate programs to collect and evaluate operating data for on-line adjustments.</li>
<li>Perform operational tests and fault isolation on systems.</li>
</ul>
Essential Skills
<ul>
<li>0-2 years of manufacturing experience preferred.</li>
<li>Good attendance and reliability.</li>
<li>Comfortable working with a microscope for 4-6 hours per day.</li>
<li>Comfortable working in a cleanroom and regulated environment.</li>
<li>Good hand-eye dexterity and experience with small hand tools.</li>
<li>Attention to detail and ability to read drawings.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>High School diploma or equivalent.</li>
<li>Basic mathematical calculation skills.</li>
<li>Experience with microscopes.</li>
<li>Ability to follow GMPs using Standard Operating Procedures.</li>
<li>Basic understanding of electricity.</li>
<li>Familiarity with Microsoft Office products.</li>
<li>Ability to perform repetitive work with attention to detail.</li>
</ul>
Why Work Here?
Our financially stable company offers large contracts with ample work and uncapped overtime. We provide opportunities for growth, as many in leadership roles began as operators. We invest in employees who are passionate and eager to learn, offering career advancement to those who show curiosity and a desire to grow.
Work Environment
Work in a clean and regulated environment with a friendly, hard-working culture. Engage in repetitive tasks, with a full gowning process required. Train on the 1st shift from 5 AM to 3:30 PM, transitioning to the 2nd shift from 3 PM to 1:30 AM, Monday through Thursday.
Job Type &amp; Location
This is a Contract to Hire position based out of Billerica, Massachusetts.
Pay and Benefits
The pay range for this position is $21.00 - $22.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Billerica,MA.
Application Deadline
This position is anticipated to close on Aug 31, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Cleanroom Assembler

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite Position in NEFSC Facility and aboard research vessels in Northwest Atlantic Ocean
*Proposal Effort, Position is Subject to Contract Award
POSITION DESCRIPTION:
Think Tank is seeking a Field Scientist to support NOAA with collaborative fisheries research with commercial fishermen. NOAA conducts diverse projects, including the Study Fleet, Gulf of Maine Bottom Longline Survey, Hook and Line Survey, Industry-Based Biological Sampling, and Environmental Monitoring programs.
This position supports both shore-side and at-sea research-from data collection and equipment maintenance to training, outreach, and scientific reporting. The role involves working closely with fishing industry partners, scientists, and vessel crews to improve fisheries data collection and advance ecosystem-based management.
RESPONSIBILITIES:
<ul>
<li>Support CRB research in field and lab, including equipment deployment, data collection, and protocol compliance.</li>
<li>Provide technical assistance at sea and ashore: troubleshoot data systems, train fishermen, and maintain sampling standards.</li>
<li>Participate in research trips (~40 sea days/year, 1–10 days each) aboard commercial vessels; coordinate with captains and crews.</li>
<li>Collect, sort, and process fish/invertebrates; conduct biological sampling (age, growth, maturity, genetics, diet).</li>
<li>Maintain and repair field equipment, fishing gear, and survey technology.</li>
<li>Serve as Chief Scientist on Gulf of Maine Bottom Longline Survey cruises, leading scientific teams and vessel operations.</li>
<li>Collect, analyze, and audit biological, fisheries, environmental, operational, and video data.</li>
<li>Manage and troubleshoot data collection hardware/software; ensure QA/QC and proper database entry.</li>
<li>Deliver biological samples and documentation to research partners.</li>
<li>Contribute to protocol development, proposals, reports, and manuscripts.</li>
<li>Represent CRB at industry meetings, workshops, and scientific conferences.</li>
<li>Develop outreach materials (manuals, guides, newsletters, blogs, social media).</li>
<li>Provide weekly updates and monthly progress reports to leadership.</li>
<li>Assist with staff training and mentoring; work independently with minimal supervision.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Bachelor's degree in fisheries, biological sciences, or equivalent professional experience.</li>
<li>3+ years field/research experience in fisheries or marine science.</li>
<li>Strong background in biological sample collection, fish identification, and data processing.</li>
<li>Proven ability to work independently and lead or support teams in challenging field conditions.</li>
<li>Demonstrated experience working with commercial fishermen and at-sea environments.</li>
<li>Experience with electronic data collection tools and troubleshooting hardware/software.</li>
<li>Strong written and verbal communication skills.</li>
<li>Proficiency with MS Office and Google Workspace (Docs, Sheets, Drive, etc.).</li>
<li>Specific Certifications will be required</li>
</ul>

Field Scientist

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Onsite at a NEFSC and aboard research vessels in the Northwest Atlantic Ocean
*Proposal Effort, Position is Subject to Contract Award
POSITION DESCRIPTION:
Think Tank is seeking a motivated Biological Technician Level II to support the NEFSC fishery-independent research surveys in the Northwest Atlantic Ocean. These positions play a vital role in assessing the abundance, distribution, and diversity of fish and invertebrate species.
Technicians will participate in extended sea-going research cruises, assist with at-sea and shore-based biological sampling, maintain advanced survey equipment, and ensure high-quality data collection to support NOAA Northeast Fisheries Science Center (NEFSC) research programs.
RESPONSIBILITIES:
<ul>
<li>Support annual research cruises (60–120 days at sea) by collecting biological and physical survey data.</li>
<li>Sort, identify, measure, and dissect fish and invertebrates; collect biological samples (age, growth, maturity, genetics, diet).</li>
<li>Operate and maintain data acquisition systems, acoustic/optical survey equipment, and sampling hardware.</li>
<li>Assist with vessel staging, gear inspection, supply preparation, and equipment calibration.</li>
<li>Perform QA/QC of survey data, manage fisheries databases, and maintain sampling inventories.</li>
<li>Annotate benthic imagery, process lab samples, and contribute to protocol development.</li>
<li>Develop outreach materials (manuals, newsletters, social media content) and support staff training.</li>
</ul>
REQUIREMENTS:
<ul>
<li>2+ years experience identifying Northwest Atlantic fish and invertebrate species.</li>
<li>Experience aboard research vessels conducting fishery-independent surveys.</li>
<li>1+ year experience with bottom trawls and/or scallop/clam dredges.</li>
<li>1+ year experience with fishery sampling hardware (measuring boards, motion-compensated scales, barcode systems).</li>
</ul>

Biological Technician Level II

<h3>Job Description</h3>
Job Description
*US Citizenship Required
*Remote Position with occasional domestic and international travel
*Proposal Effort, Position is Subject to Contract Award
POSITION DESCRIPTION:
NEFSC conducts vital research on Atlantic salmon and other fish species to inform conservation, management, and habitat restoration. Think Tank is seeking a Fisheries Research Analyst Level III to join our collaborative team and support a wide range of technical, analytical, and field projects.
This role combines field research, laboratory work, data analysis, and technical writing to advance the conservation of Atlantic salmon and other diadromous fish, such as American eel, river herring, shad, striped bass, and rainbow smelt. Analysts will work closely with federal, state, tribal, academic, and international partners to assess habitat quality, evaluate management strategies, and support domestic and international sampling programs.
RESPONSIBILITIES:
<ul>
<li>Conduct data synthesis, statistical analysis, and reporting on salmon and other fish population dynamics, habitat quality, and ecology.</li>
<li>Support development of management strategies, models, and user interfaces; contribute to technical reports and peer-reviewed publications.</li>
<li>Process and archive fish scale samples; support automation/machine learning for data efficiency.</li>
<li>Maintain databases, geo-spatial layers, analysis code, and technical documentation.</li>
<li>Participate in domestic and international fieldwork, including trawl surveys, trap/electrofishing monitoring, and salmon sampling.</li>
<li>Prepare, ship, and manage sampling kits and biological materials.</li>
<li>Travel up to 8 weeks/year for field assignments.</li>
<li>Work with state, tribal, federal, academic, and international partners.</li>
<li>Present findings at scientific meetings and workshops.</li>
<li>Provide monthly reports, synthesis notes, and updates to project leads.</li>
</ul>
REQUIREMENTS:
<ul>
<li>Ph.D. in relevant field (or M.S. with 6+ years post-degree experience).</li>
<li>Demonstrated leadership in research projects and team management.</li>
<li>Strong expertise in advanced statistical modeling and population analysis.</li>
<li>Experience with computerized data entry and data auditing.</li>
<li>Medical clearance and safety certifications (as required for fieldwork).</li>
<li>Experience collaborating with state, tribal, and academic partners.</li>
<li>Demonstrated technical and scientific writing experience (preferably with publications).</li>
<li>Proficiency with statistical software (R, Matlab, Statgraphics, or similar).</li>
<li>First Aid/CPR certification (Red Cross or American Heart Association).</li>
<li>Valid driver's license and passport (6+ months from task completion).</li>
<li>Proficiency in Microsoft Office and Google Workspace tools.</li>
<li>Strong time management, attention to detail, and communication skills.</li>
<li>Ability to adapt to changing priorities and work independently or in teams.</li>
<li>Willingness to travel domestically (1–4 weeks at a time) and internationally (up to 3 weeks annually).</li>
</ul>

Fisheries Research Analyst Level III

<h3>Job Description</h3>
Job DescriptionThe Company We are Alloy Therapeutics—a biotechnology ecosystem company empowering the global scientific community to make better medicines together. Through a community of partners, we democratize access to pre-competitive tools, technologies, services, and company creation capabilities that are foundational for discovering and developing therapeutic biologics. The company facilitates affordable, non-exclusive access to the entire drug discovery community from academic scientists, small and medium biotech, to the largest biopharma. At Alloy, we believe our industry should compete on getting the best drugs to patients as quickly as possible, not exclusive access to the best platforms. As a reflection of our relentless commitment to the scientific community, we reinvest 100% of our revenue in innovation and access to innovation. MAY THE BEST DRUG WIN. Alloy is headquartered in Waltham, MA with additional labs in Cambridge, UK; Basel, Switzerland, and Athens, GA. Successful members thrive in our shared culture of accountability, deliberate trust, and open communication. As a team we aspire to work together to exceed expectations and collectively contribute across the global organization to always maintain our nimble, startup culture. This is an on-site and full-time position in Waltham, MA. At Alloy, we have an ethos of “Mentorship-By-Apprenticeship” in all of our positions.&nbsp;&nbsp;We strive to have workers in the office when needed to interact organically and face-to-face.&nbsp;&nbsp;Of course, as a lab-based operation, our cells and animals grow 7 days a week, 365 days per year.&nbsp;&nbsp;We respect and value our colleagues for their hard work that requires them to be in the lab every day.&nbsp;&nbsp;We ask our people who have more flexible accommodations, like this position, to appreciate their colleagues who have less flexibility.&nbsp;&nbsp;We are all one team! The Team The In Vitro Discovery team is a collaborative group driving antibody discovery and optimization using cutting-edge technologies. We work cross-functionally to advance therapeutic solutions, maintaining scientific rigor and efficiency in a fast-paced environment. The Role As an Associate Scientist, you will contribute to antibody discovery and optimization campaigns using state-of-the-art in vitro platforms. This role requires a highly motivated and detail-oriented individual with a strong background in molecular biology and antibody discovery techniques. You will collaborate closely with cross-functional teams to advance projects and deliver high-quality results. This role will report to the head of in vitro discovery and optimization, with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.&nbsp; How You’ll Drive Impact
<ul>
<li>Advance antibody discovery and optimization efforts through innovative in vitro strategies</li>
<li>Deliver high-quality experimental data supporting lead identification and engineering.</li>
<li>Foster effective cross-functional collaboration and communication.</li>
<li>Manage multiple projects with scientific rigor and organizational efficiency.</li>
<li>Contribute to Alloy’s culture of innovation and teamwork.&nbsp;</li>
</ul>
Principle responsibilities
<ul>
<li>Design, execute, and analyze experiments to support antibody discovery and engineering.</li>
<li>Collaborate closely with cross-functional teams to align project goals and timelines.</li>
<li>Document and communicate experimental findings clearly to stakeholders and teams.</li>
<li>Contribute to the development and optimization of in vitro platforms and workflows.</li>
<li>Manage multiple projects simultaneously, maintaining high scientific standards.</li>
<li>Provide technical expertise in molecular biology and related techniques.</li>
<li>Support high-throughput screening and assay development efforts.</li>
<li>Participate in regular team meetings and contribute to strategic planning.</li>
<li>Stay up to date with emerging technologies and scientific advances in the field.</li>
<li>Maintain an organized and efficient laboratory environment.</li>
</ul>
Qualifications
<ul>
<li>Minimum of 5 years of related experience with a Bachelor’s degree; or 3 years and a Master’s degree</li>
<li>Hands-on experience in molecular biology techniques (e.g., cloning, PCR, sequencing).</li>
<li>Hands-on experience with yeast/phage/mammalian display platforms</li>
<li>Strong organizational and communication skills to work effectively in collaborative settings.</li>
<li>Demonstrated ability to manage timelines and contribute to multiple projects in parallel.</li>
<li>Preferred experience with cell culture, flow cytometry,&nbsp;NGS sequencing and high-throughput screening</li>
<li>&nbsp;Ability to work across various US and international time zones.</li>
</ul>
Taking Care of Our People We support the individuality of what people need to do outside of work to empower them to do their best at work. While you focus on making better medicine together, we focus on programs and benefits that support a diverse and growing team. Whether you’re single, in a growing family, or nearing retirement, Alloy offers a variety of comprehensive and competitive benefits starting from day one. Compensation
<ul>
<li>Competitive base and equity compensation commensurate with level of experience and independence</li>
<li>401(k) company match</li>
</ul>
Health &amp; Family
<ul>
<li>Generous personal and family medical, dental and vision benefits with 100% of premiums and deductibles covered</li>
<li>Company-paid disability (STD, LTD) and life insurance</li>
<li>Paid parental leave</li>
<li>Family planning support up to $45,000 (e.g., IVF/PGT, adoption, surrogacy, egg retrieval)</li>
</ul>
Unique Perks
<ul>
<li>Unlimited PTO (paid time off) and flexible schedules</li>
<li>Annual stipend for continuing education with commitment to your career through individualized professional development plan</li>
<li>Wellness and Extensive Employee Assistance Program (EAP) including resources for mental wellness</li>
</ul>
Pay Transparency At Alloy Therapeutics, we believe in fostering trust and open communication. For this role, the estimated annual base salary range is $94,500 - $104,000, with the final offer based on factors like your experience, skills, and alignment with our needs.
Additionally, this role is eligible for equity compensation, reflecting our commitment to shared success as we work together to make better medicines.
We are proud to offer competitive compensation and benefits, aiming to support our team’s professional and personal well-being. If you have any questions about pay or benefits, we’re here to help.
Alloy Therapeutics is an equal opportunity employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, veteran status, disability, or other legally protected status.&nbsp; If you are unable to submit an application because of incompatible assistive technology or a disability, please contact us at <a href="mailto:recruiting@alloytx.com" target="_blank">recruiting@alloytx.com</a>.&nbsp; We will make every effort to respond to your request for disability assistance as soon as possible. &nbsp;
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7DYUTtBc3V

Associate Scientist, In Vitro Discovery

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting to the Associate Director of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of research operations focused on pipeline advancement and evaluation. The Senior Research Associate I / II will be responsible for conducting immunogenicity assays to measure the efficacy of clinical vaccines and work closely with teammates on the organizations Translational Medicine team. Additional functions of the role include performing in vivo mouse experiments to characterize the immune response to the companys lead vaccine candidates.
Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts, with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States.
 Major Duties/Responsibilities
<ul>
<li>Execute immunogenicity and/or biomarker assays to evaluate correlates of response to therapeutic vaccination, such as ELISPOT/Fluorospot, ICS, and other flow cytometry-based assays</li>
<li>Complete experimental documentation and data analysis following appropriate SOPs for investigations on clinical samples</li>
<li>Perform PBMC isolations from whole blood and leukopak for research and clinical studies</li>
<li>Review and author compliant documents as part of the organizations document life cycle management</li>
<li>Assist with clinical sample management, including sample receipt and maintenance of the clinical sample chain of custody</li>
<li>Perform murine handling, injections, and blood/organ collections</li>
<li>Communicate findings in various forums and interact collaboratively with other team members</li>
<li>Willingness to learn new analytical assays and assist with the advancement of novel T cell and antibody-based assays</li>
<li>Perform job responsibilities in compliance with GCLP guidelines, where applicable</li>
</ul>
Education &amp; Professional Experience
<ul>
<li>BS with 3-5+ years of relevant work experience OR MS with 1-3+ years of experience</li>
<li>Ability to take initiative and produce in a fast-paced environment</li>
<li>Ability to prioritize tasks and consistently demonstrate strong decision-making and judgment skills</li>
<li>Strong attention to detail, organizational skills, and the ability to manage multiple projects</li>
<li>Outstanding communication (written and verbal) and interpersonal skills</li>
<li>This position is based in our Boston office and requires on-site presence</li>
</ul>
Working Conditions
<ul>
<li>Busy office/laboratory environment with frequent deadlines and interruptions</li>
</ul>
 
Travel
<ul>
<li>Travel is not required</li>
</ul>
 
Physical Requirements
<ul>
<li>Subject to periods of sitting or standing, vision is required to monitor data. Work is performed exclusively in an office/laboratory environment.</li>
</ul>
 
About Elicio Therapeutics
Elicio Therapeutics, Inc. (Nasdaq: ELTX) is a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of high-prevalence cancers, including mKRAS-positive pancreatic and colorectal cancers. Elicio intends to build on recent clinical successes in the personalized cancer vaccine space to develop effective, off-the-shelf vaccines. Elicios Amphiphile (AMP) technology aims to enhance the education, activation and amplification of cancer-specific T cells relative to conventional vaccination strategies, with the goal of promoting durable cancer immunosurveillance in patients. Elicios ELI-002 lead program is an off-the-shelf vaccine candidate targeting the most common KRAS mutations, which drive approximately 25% of all solid tumors. Off-the-shelf vaccine approaches have the potential benefits of low cost, rapid commercial scale manufacturing, and rapid availability of drug to patients especially in neo-adjuvant settings and for prophylaxis in high-risk patients, contrary to personalized vaccines approaches. ELI-002 is being studied in an ongoing, randomized clinical trial in patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. ELI-002 also has been studied in patients with mKRAS-positive colorectal cancer (CRC) in Phase 1 studies. The updated AMPLIFY-201 Phase 1 data for PDAC and CRC was presented at the ESMO Immuno-Oncology Congress 2024 and included a 16.3-month median recurrence-free survival and 28.9-month median overall survival for the full study population. In the future, Elicio plans to expand ELI-002 to other indications including mKRAS positive lung cancer and other mKRAS positive cancers. Elicios pipeline includes additional off-the-shelf therapeutic cancer vaccines candidates, including ELI-007 and ELI-008, that target BRAF-driven cancers and p53 hotspot mutations, respectively. For more information, please visit <a href="http://www.elicio.com" target="_blank">www.elicio.com</a>.
 
About the Amphiphile Platform 
Elicios proprietary AMP platform delivers investigational immunotherapeutics directly to the brain center of the immune system the lymph nodes. Elicio believes this site-specific delivery of disease-specific antigens, adjuvants and other immunomodulators may efficiently educate, activate and amplify critical immune cells, potentially resulting in induction and persistence of potent adaptive immunity required to treat many diseases. In preclinical models, Elicio observed lymph node-specific engagement driving therapeutic immune responses of increased magnitude, function and durability. Elicio believes its AMP lymph node-targeted approach will produce superior clinical benefits compared to immunotherapies that do not engage the lymph nodes based on preclinical studies.
 
Elicios AMP platform, originally developed at the Massachusetts Institute of Technology, has broad potential in the cancer space to advance a number of development initiatives through internal activities, in-licensing arrangements or development collaborations and partnerships.
 
The AMP platform has been shown to deliver immunotherapeutics directly to the lymph nodes by latching on to the protein albumin, found in the local injection site, as it travels to lymphatic tissue.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionJob Description The Role: Title: In vivo research associate, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated in vivo research associate to support in vivo experiment (rodent), including MTD studies, Efficacy studies, PK/PD studies and tissue harvest. You will also be asked to maintain and expand cancer cell lines to support the in vivo tumor model studies and conduct hand-on dosing and procedure support for mice pharmacology studies. In addition, you may need to support all aspects of laboratory operation to maintain a highly productive vivarium/laboratory. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Hand-on execute subcutaneous tumor model studies from cancer cells expansion, implantation (in mice), tumor measurement, group randomization and administration of test articles. </li>
<li>Hand-on support all mice pharmacology study procedures, including but not limiting to dosing and tissue harvest.</li>
<li>Follow PIRC IACUC program/protocols and standard operating procedures (SOPs) for all animal procedures.</li>
<li>Maintain and expand cancer cell lines for human xenograft tumor and mouse syngeneic tumor models. </li>
<li>Data process and graphing for the internal team update presentation.</li>
</ul>
Essential Qualifications:
<ul>
<li>B.S. or higher degree in immunology, pharmaceutical sciences or related scientific field</li>
</ul>
&nbsp;SkillPerformed in the last 2 years (includes training)In vitro assayELISANot required, good to knowMSDNot required, good to knowFACSNot required, good to knowHusbandry&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Aseptic TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Micro-Isolator TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Restraint &amp; HandlingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Room ChecksNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cage ChangeNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Injections/ Administration&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubcutaneousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntraperitonealMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntravenousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntramuscularNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oral GavageNot required, good to knowBlood Withdrawal&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tail BleedMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cardiac PunctureMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubmandibularMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; RO BleedNot required, good to knowEuthanasia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; CO2 OverdoseMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cervical DislocationMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; DecapitationNot requiredAnimal Preparation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ShavingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear TaggingNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear Punching/ NotchingNot requiredImplantation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Xenograft SCMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mammary Fat Pad&nbsp;Good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; TrocarNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Anesthesia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Isoflurane AnesthesiaNot required, good to knowLab OperationsGeneral Organizing lab spaceMustReceiving/stocking suppliesMustAny other duties that may ariseMustMammalian Cell CultureStandard mammalian cell culture procedures and associated aseptic techniques in addition to maintenance of tissue culture facilitiesMustMedia and buffer preparation, culture initiation, propagation, and cryopreservation of cells, including primary human and mouse cells and cell lines as well as adherence to quality control schedules for ensuring consistency of cell culture materials.Must &nbsp; EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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In-vivo Research Associate, Immunology and Pharmacology

<h3>Job Description</h3>
Job DescriptionJob Title: Process Chemistry Contractor Location: Cambridge, MA, 02139 Duration:12+ months (Possibilities of Extension) Work Shift: : 5 days onsite in the lab. Pay Rate: $43/Hour on W2 Job Description Summary: Duties: Seeking an exceptional organic chemist to join our Process Chemistry group. This contract position resides within the Pharmaceutical Sciences organization. The candidate will work full-time onsite and execute laboratory activities related to the development of robust drug substance manufacturing processes across various phases of drug substance development. The ideal candidate will conduct multi-step organic synthesis, route scouting and optimization, purification and characterization of intermediates and final compounds to support drug substance scale-up activities. An ideal candidate will have a strong foundation in modern synthetic organic chemistry and analytical techniques such as NMR, LCMS, UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments. Experience in small-molecule process development and scale up is highly desired, however not required. Responsibilities: • Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member. • Collaborate with cross-functional teams to ensure successful project outcomes. • Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes. • Document and report experimental results and findings. • Draft and review technical documents (development reports, patent applications, tech transfer documents etc.) • Maintain an accurate, timely and compliant laboratory notebook. • Maintain laboratory equipment and ensure compliance with safety regulations. Skills: Qualifications: • Strong knowledge of organic chemistry. • Experience with early phase route development and process optimization • Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software. • Strong analytical and problem-solving skills. • Strong written and verbal communication skills. • Ability to work independently and as part of a team. • Strong organizational and time management skills. Capabilities: • Ability to effectively prioritize and manage multiple tasks and compounds • Ability to adapt to change and to work optimally within a variety of situations • Ability to build productive working relationships across functions and highly diverse groups of individuals • Self-motivated and willing to “learn on the job” and ask for assistance when needed • Ability to make a significant impact in a results-driven environment where accountability is key. • A team player, who listens effectively and invites response and discussion • A collaborator who communicates in an open, transparent, complete, timely and consistent manner Education: 
<ul>
<li>An ideal candidate would have a B.S. or M.S. in Chemistry, or a related field with 3+ years of experience in pharmaceutical research or laboratory setting or, Ph.D. with 0-3 years of experience.</li>
</ul>
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