field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Join a fast-paced, hands-on cannabis team where quality, consistency, and collaboration are central to daily operations. The Post Processing Technician 3 works Tuesday through Sunday from 7:00 AM to 5:30 PM and plays a key role in supporting and coordinating day-to-day processing activities while remaining actively involved in hands-on production work. Under the direction of the Processing Supervisor, this position supports harvest activities, green waste disposal, batch bucking, trimming, inspections, sorting, quality control, and oversight of dry and cure processes, as well as inventory management within trim, dry, and cure areas.
This role supports daily workflow by training team members on routine post-processing tasks and helping assign and monitor work to maintain efficiency and quality standards. The Post Processing Technician 3 performs processing tasks across all areas while ensuring compliance with established SOPs and operational guidelines and assists with developing and updating departmental SOPs as needed. The position also supports scheduling and production planning efforts, identifies and helps resolve workflow or production issues, and collaborates with leadership and HR on performance-related matters when necessary.
The ideal candidate is detail-oriented, adaptable, and comfortable working in a structured yet fast-moving environment. Strong verbal and written communication skills and the ability to maintain clear, respectful communication with peers and management are essential. This role requires the ability to stand for extended periods on concrete floors, frequently walk and reach, regularly lift 10-20 pounds with occasional lifting up to 50 pounds, and perform tasks requiring fine motor skills, balance, and physical movement such as stooping, kneeling, and climbing ladders or stairs. Previous experience is preferred but not required; training will be provided for the right candidate. Think you would be a good fit? Apply Today!

Post Processing Technician 3

<h3>Job Description</h3>
A recognized pharma company is hiring a Senior Analyst I, Quality Control Chemistry on a one-year contract basis near Boston, MA. 
**This position is for candidates who are able to work on a W2 basis.**
Responsibilities: 
<ul>
<li>Execute analytical test methods to support product release and stability of AAV products using different analytical techniques (e.g. HPLC, LCMS, AUC, UV, CE-SDS, compendia methods like Osmolality, pH, Sub visible particulates and Appearance)</li>
<li>Review and approval of cGMP analytical data for release and stability testing from chemistry analytical test methods</li>
<li>Supports and leads QC Chemistry laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc).</li>
<li>Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as needed</li>
<li>Write, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methods</li>
<li>Perform other duties, as needed</li>
</ul>
Qualifications:
<ul>
<li>5+ years of experience working in cGMP environment</li>
<li>Bachelor's and/or Master's Degree in Analytical Chemistry, Biochemistry, Biophysics, or a related discipline</li>
<li>Experience working in the cGMP QC lab of the Pharmaceutical or Biopharmaceutical industry </li>
<li>Experience working with external contract labs (CMOs, CROs)</li>
</ul>
Desired Skills:
<ul>
<li>Experience analyzing Nucleic Acids, Virus Capsids, Antibodies, and/or other Biologics materials using HPLC/UPLC, LCMS, AUC, UV- Vis, CE-SDS </li>
</ul>

Senior Analyst I, Quality Control Chemistry

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>
Seeking a highly motivated individual to join our team as a Compound Hub Specialist.
</li>
<li>
As a key contributor within our team, you will play a crucial role in processing new compounds and inventory requests through the Compound Hub Process while prioritizing customer satisfaction and order maintenance.
</li>
<li>
As a member of the Sample Management group, your primary responsibilities will include:
</li>
<li>
Handling all new compound orders, weighing solid samples within a weigh hood using an analytical balance to create solutions for customers, including local chemists and biologists.
</li>
<li>
Utilizing the Tecan Liquid Handler to process compound orders efficiently and accurately.
</li>
<li>
Loading Tecan products onto an automatic sorting system for delivery to recipients across our local sites as well as domestic and international customers.
</li>
<li>
Receiving samples from both internal and external locations and ensuring all service level agreements are achieved on a daily basis, collaborating closely with scientific staff to prioritize important orders.
</li>
<li>
Engaging with customers directly to understand their needs, address inquiries, and provide exceptional service throughout the order fulfillment process.
</li>
</ul>
Skills and Qualifications:
<ul>
<li>
Bachelor's degree with experience working in a scientific lab, emphasizing compound inventory management and distribution using automated systems.
</li>
<li>
Thorough knowledge of compound management activities, including inventory management, solution production, quality control, and logistics management.
</li>
<li>
Experience working with laboratory robotics, including diagnosing and troubleshooting hardware and software issues.
</li>
<li>
Excellent personal and communication skills, with a strong focus on customer satisfaction and maintaining professional relationships.
</li>
<li>
Ability to multitask in a fast-paced environment, prioritize workload effectively, and work well within a team.
</li>
<li>
Self-motivated, well-organized, and reliable individual with a customer-focused mindset.
</li>
<li>
Proficiency in MS Office products, including File Explorer and other relevant software tools.
</li>
<li>
Service-oriented mindset with a keen attention to detail and the ability to interact effectively with scientific staff.
</li>
<li>
Knowledge of instrumentation/systems such as Tecan evo, Biomicrolab Volume Checker, and Biomicrolab Tube Sorter.
</li>
<li>
Prefer 6-18 months of relevant experience in a similar role.
</li>
<li>
Sample/Chemical management experience.
</li>
<li>
Shift timings: Monday to Friday, 7 am - 4 pm
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

Associate Scientist - Compound Hub Specialist

<h3>Job Description</h3>
Background
Hamad Medical Corporation (HMC) occupies a central position within Qatar’s rapidly expanding biomedical and clinical research ecosystem. As the nation’s leading public healthcare provider, HMC carries a dual mandate: to deliver exemplary patient care and to advance scientific innovation that shapes the future of health in Qatar. Over the past decade, HMC has cultivated one of the region’s most comprehensive research environments, an ecosystem intentionally designed to promote discovery, foster collaboration, and accelerate the translation of scientific advances into clinical practice. 
At the core of this environment is the Medical Research Center (MRC), which provides institutional research governance, promotes adherence to ethical standards, and supports skill development across all HMC facilities. Through its dedicated research units, biostatistical support structures, clinical-trial frameworks, and internal funding programs, the MRC empowers investigators, physicians, nurses, scientists, and allied health professionals to conduct rigorous, patient-centered research that addresses national and global health priorities. 
Summary 
We seek an accomplished scientific leader to serve as Director of TRI. The Director will set and execute the Institute’s vision; build high-performing, diverse teams; and deliver a robust pipeline of translational programs through preclinical development and into early clinical evaluation. The Director reports to the Chief of Scientific, Academic and Faculty Affairs and serves as the primary ambassador to government entities, healthcare systems, universities, and industry partners.
Key Responsibilities
Strategy &amp; Governance
<ul>
<li>Develop and deliver a multi‑year scientific and translational strategy aligned to national health priorities and international best practice.</li>
<li>Oversee research governance, research integrity, biosafety, and compliance frameworks.</li>
<li>Lead annual planning, portfolio reviews, and transparent KPIs.</li>
</ul>
Research Portfolio &amp; Cores
<ul>
<li>Build and manage an agile portfolio spanning target discovery, biomarker platforms, preclinical models, and early‑phase clinical translation.</li>
<li>Oversee shared research cores (e.g., preclinical models, genomics/proteomics/metabolomics, bioinformatics, biobanking, imaging) with service-level metrics.</li>
</ul>
Clinical &amp; Industry Translation
<ul>
<li>Contribute to establishing pipeline routes from discovery to IND/IDE-enabling studies and early clinical trials in partnership with Clinical Trial Unit.</li>
<li>Drive robust biomarker and patient‑stratification strategies; champion reproducibility and data standards.</li>
<li>Foster industry collaborations, licensing, sponsored research, and venture creation with technology transfer partners (patents, licensing, industry collaboration).</li>
</ul>
People &amp; Culture
<ul>
<li>Recruit, mentor, and retain best investigators and professional staff; embed inclusive, collaborative, and high-performance culture.</li>
<li>Advance training programs in translational methods, GxP awareness, and clinical research.</li>
</ul>
Funding &amp; Partnerships
<ul>
<li>Secure diversified funding (government, competitive grants and industry).</li>
<li>Build strategic partnerships across Doha and internationally with ability to align TRI strategy and outputs with Qatar’s national health and research priorities; represent TRI in national and global consortia </li>
</ul>
Operations &amp; Infrastructure
<ul>
<li>Ensure efficient operations, budget stewardship, and risk management across labs, cores, and clinical interfaces.</li>
<li>Champion modern informatics (FAIR data, LIMS/ELN, secure compute, and responsible AI) and open, ethical data‑sharing.</li>
</ul>
Candidate Profile
<ul>
<li>Doctoral degree (PhD, MD, or MD/PhD) in a relevant biomedical field.</li>
<li>Internationally recognized record of translational research leadership and impact (e.g., advancing assets to IND/first‑in‑human, pivotal biomarkers, or clinical proof‑of‑concept).</li>
<li>Experience leading multidisciplinary teams and shared research facilities; demonstrated ability to scale programs and deliver measurable outcomes.</li>
<li>Deep familiarity with preclinical translation, experimental medicine, clinical trial interfaces, and GxP expectations (GLP/GCP/GMP awareness).</li>
<li>Evidence of successful partnerships with clinicians, healthcare systems, regulators, and industry; track record in securing significant funding.</li>
<li>Commitment to research integrity, diversity and inclusion, and talent development.</li>
<li>Excellent communication, stakeholder engagement, and change-management skills.</li>
<li>Experience in clinical trial interfaces, patient-stratification, and translation of biomarkers into clinical protocols </li>
</ul>
 
Job Location: Doha Qatar

Principal Research Scientist-Director, Translational Research Institute (Doha)

<h3>Job Description</h3>
Job Description
Ophthalmic Consultants of Boston is a group practice specializing in eye care.&nbsp;Our Physicians are actively involved in research that is advancing the understanding of many eye conditions.&nbsp; We conduct numerous clinical trials aimed at finding new treatments for many eye conditions, so that we are able to offer the best treatment options to our patients. Are you looking for Patient interaction in your next Research Role?&nbsp;We are currently hiring Research Coordinator/Technician to join our team. This is a full-time (Monday - Friday) on-site position. The hours are 7:30AM-4:00PM. Travel to Boston, Waltham, and Weymouth are required.
Summary of duties: Responsible for the coordination of multiple research studies. Responsibilities include preparation of study materials, overseeing participant enrollment, coordinating participant visits pursuant to study protocol, and completion of required verbal and written communication with study sponsor.
Responsibilities:
<ul>
<li>Actively applies knowledge&nbsp;</li>
<li>Performs other research-related duties as needed</li>
<li>Ability to work professionally and effectively with patients, as well as clinical and administrative staff</li>
<li>Strong interpersonal and communication skills</li>
<li>Excellent organization, planning and prioritizing capabilities</li>
<li>Exercise initiative and take responsibility.&nbsp;</li>
<li>Work requires continuous attention to detail in all responsibilities.&nbsp;&nbsp;</li>
</ul>
Education and Experience Preferred:
<ul>
<li>Bachelors of Science degree preferred.</li>
<li>1-2 years of experience as an ophthalmic technician.</li>
<li>Ideal candidates will have experience in high volume ophthalmic environment.</li>
<li>Knowledge of clinical research procedures.</li>
</ul>
 Benefits Offered:
<ul>
<li>Health &amp; Dental Insurance- starts 1st Day of Employment</li>
<li>Paid time off and Paid Holidays</li>
<li>Health &amp; Dependent Reimbursement Accounts</li>
<li>401(k) Plan with Company Contribution</li>
<li>Co. paid Life and LTD Insurance</li>
<li>Employee Discounts</li>
</ul>
To find out more about OCB, please visit our website at <a href="http://www.eyeboston.com.&amp;nbsp" target="_blank">www.eyeboston.com.&amp;nbsp</a>; OCB is an Equal Opportunity Employer.
Powered by JazzHR
OP5r7kf9ss

Research Coordinator

<h3>Job Description</h3>
Job Description
Organization Overview
The National Institute for Children’s Health Quality (NICHQ) is a mission-driven nonprofit dedicated to driving dramatic and sustainable improvements in the complex issues facing children’s health. We provide deep expertise in building and managing effective change strategies that align partners and engage participants to achieve better outcomes for children’s health. 
Position Overview 
The Senior Analyst brings knowledge of and experience in applied research and evaluation and applies that knowledge to lead the successful design, execution and management of projects in the context of NICHQ’s maternal child health work. The Senior Analyst works closely and collaboratively with the Senior leadership in Programs and in the Department of Applied Research and Evaluation (DARE), project leads, Quality Improvement Advisors, expert faculty members, funders, and project teams to design and execute applied research and evaluation work that provides high-quality, relevant data analysis and recommendations across the lifecycle of projects. The Senior Analyst plays an integral and leadership role on NICHQ’s Applied Research and Evaluation team, guiding the department’s work (under the supervision of the Associate Director and senior leadership in DARE), as well as in the team’s work to capture, develop, and spread innovative approaches. The Senior Analyst may provide additional research consulting services and assist in elevating NICHQ’s standing in the scientific community by driving strategic planning for publications and conference presentations. 
Summary 
Career Level: Experienced 
Status: Full-Time, Exempt Employee, US Based Remote
Education: Master’s degree required; doctoral degree in relevant discipline preferred 
Reports to: Principal Analyst Department of Applied Research and Evaluation (DARE) 
Salary: $84,000 
Responsibilities 
<ul>
<ul>
<li>Applied research and evaluation tasks including
<ul>
<li>Planning
<ul>
<li>Create and implement plans for data management and analytic file creation</li>
<li>Collaborate with program staff to meet project deliverables on schedule</li>
</ul>
</li>
<li>Data collection and management
<ul>
<li>Design, build and maintain REDCap databases to support research data collection efforts</li>
<li>Create and optimize data collection instruments ensuring alignment with research objectives and reporting requirements</li>
<li>Develop and implement data collection protocols, including date entry guidelines, access controls and validation rules</li>
<li>Establish and maintain quality assurance and quality control systems</li>
<li>Perform data validation checks and produce reports for internal teams and external stakeholders</li>
<li>Investigate, track, and resolve data queries, support extant data transfer efforts</li>
<li>Lead data harmonization efforts across data sources</li>
<li>Provide technical guidance and support on REDCap functionalities and best practices to project teams</li>
</ul>
</li>
<li>Data analysis
<ul>
<li>Clean, transform, and validate data to ensure accuracy and readiness for analysis</li>
<li>Conduct descriptive and inferential analysis using statistical software such are SAS to inform research findings</li>
<li>Utilize knowledge of statistical methodology to inform study design and operations.</li>
<li>Provide consultation to other project teams on statistical analysis techniques (e.g., sampling, random assignment, application scoring and weighting), as needed</li>
<li>Keep abreast of current trends in statistical methods and program evaluation</li>
</ul>
</li>
<li>Reporting and dissemination
<ul>
<li>Prepare comprehensive summaries and graphic representations of statistical findings across different formats</li>
<li>Review abstracts for professional conferences and manuscripts for peer-reviewed publications</li>
<li>Provide consultation to project teams in their development of reports and other materials that include research data</li>
</ul>
</li>
</ul>
</li>
<li>Identifies and appropriately brings complex project insights, concerns, and potential solutions in a timely manner to project and DARE lead(s) and collaborates to implement solutions</li>
<li>May be responsible for the supervision and development of individuals working in applied research and evaluation</li>
<li>Represents the Applied Research and Evaluation team on projects in a collaborative and supportive manner and participates in other activities of the applied research and evaluation team as needed</li>
</ul>
</ul>
Skills and Knowledge
<ul>
<li>Demonstrates subject matter expertise in data management, biostatistics and/or epidemiology</li>
<li>Synthesizes complex information into usable formats</li>
<li>Works independently, capable of making decisions with limited oversight</li>
<li>Ability to manage multiple projects and meet deadlines with minimal support from supervisor while working remotely</li>
<li>Strong communications skills (both verbal and written)</li>
</ul>
 Qualifications and Characteristics
<ul>
<li>Master’s degree or MPH in biostatistics or epidemiology; at least 3 years’ work experience in a health services, social science, or clinical research setting doing quantitative research</li>
<li>Experience designing, building and maintaining REDCap databases</li>
<li>Extensive experience and strong programming skills in statistical software programs (e.g. SAS and R)</li>
<li>Proficient in Microsoft Office, visualization software and database management; adept at quickly learning new technologies</li>
<li>Detail-oriented “achiever” who takes initiative</li>
</ul>
Benefits 
We offer a generous benefits package for employees including competitive compensation; US based remote work; paid time off including vacation, sick and holidays; insurance including medical, dental, vision, disability and life; flexible spending accounts; employee assistance programs; paid parental leave and professional development benefits.
NICHQ is committed to increasing the representation of people from culturally and linguistically diverse backgrounds in our workforce and to value and embrace their skills, perspectives and experiences for the benefit of our mission. NICHQ is an equal opportunity employer; all qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, gender or gender expression, sexual orientation, age marital status or disability. NICHQ strongly encourages applications from candidates who identify as BIPOC, LGBTQIA+, or from any other minoritized group.
To Apply 
To apply for this employment opportunity, please complete and submit an online application at NICHQ.org.

Senior Analyst, Applied Research and Evaluation

<h3>Job Description</h3>
Job Description
Research Associate (Pre-Award)
Join our client’s team as a pivotal force in advancing research excellence! We are seeking a dedicated and highly organized Research Associate (Pre-Award) to lead the critical early stages of sponsored research proposal development. In this essential role, you'll support faculty in navigating complex funding opportunities, ensuring proposals meet all guidelines and deadlines. This position offers a dynamic environment where your expertise will directly contribute to groundbreaking research initiatives, making a lasting impact in higher education or medical research settings. &nbsp;
Compensation: $35.00/hr *
*listed not guaranteed – potential offers vary based on experience level, qualifications, and internal equity and may be outside of this range. &nbsp;
What you'll bring to the table: a proven track record in research administration, with hands-on experience in federal agencies like NIH, NSF, DOE, or DOD. Your exceptional organizational skills, combined with a strong understanding of federal regulations and sponsor requirements, will empower you to review, refine, and submit competitive proposals. You thrive in collaborative environments, working closely with faculty and internal departments to streamline processes and secure funding success.
Candidates should possess at least five years of experience in pre-award research administration, with recent exposure to at least three of the specified federal agencies. Experience supporting faculty within higher education or medical research institutions, mastery of electronic research administration tools such as eRA Commons, Research.gov, and Grants.gov, and a comprehensive understanding of federal and institutional policies are essential. The role requires a campus presence with about 90% in-person engagement to foster effective collaboration and support.
If you're ready to make a meaningful difference in the research community and excel in a fast-paced, impactful environment, we encourage you to apply today!
Our Commitment to Inclusion &amp; Belonging The Hollister Group is an equal opportunity employer. We welcome and encourage applications from people who are under-represented in their respective occupation or position. #HGP #AM-LI1
Pandologic. Keywords: Research Associate, Location: Cambridge, MA - 02238 , PL: 600736062

Research Associate (Pre-Award)

<h3>Job Description</h3>
Job Description
Mission Summary:
We are looking for a highly motivated intern to join our Behaviors team and conduct research on Machine Learning for prediction and planning. Here, you will work with the team behind nuScenes, nuPlan, PBP Trajectory Prediction and DriveIRL to deliver ML technologies aligned with the core values of Motional, ensuring the highest standards of quality, scientific rigor and innovation.
What you'll be doing:
<ul>
<li>Conduct research on driving behavior related topics, such as motion prediction and planning, agent simulation, scenario generation, Vision-Language-Action model(VLA), etc.</li>
<li>Work with large-scale internal realworld driving datasets to demonstrate the effectiveness of your research</li>
<li>Collaborate with different teams to deploy your research results into the autonomous vehicles and test it onroad. </li>
<li>Publish the research results in papers and patents</li>
</ul>
What we are looking for:
<ul>
<li>Enrolled in a Masters or PhD program in Computer Science, Electrical Engineering, Robotics or similar technical field of study</li>
<li>Strong Machine Learning research background with publications in any of the top-tier conferences(RSS, ICRA, CoRL, CVPR, ICRL, ICML, NeurIPS, etc.)</li>
<li>Proficiency in Python coding and PyTorch or other commonly-used deep learning frameworks</li>
<li>One-team mindset and effective collaboration with other researchers and engineers</li>
<li>Strong communication and interpersonal skills</li>
<li>Previous experience in autonomous driving is preferred</li>
</ul>
Note: This will be a hybrid onsite internship position in Boston or Pittsburgh. We will accept resumes on a rolling basis until the role is filled. Compensation will be based on location and degree level. 
Motional is a driverless technology company making autonomous vehicles a safe, reliable, and accessible reality. We're driven by something more.
Our journey is always people first.
We aren't just developing driverless cars; we're creating safer roadways, more equitable transportation options, and making our communities better places to live, work, and connect. Our team is made up of engineers, researchers, innovators, dreamers and doers, who are creating a technology with the potential to transform the way we move.
Higher purpose, greater impact.
We're creating first-of-its-kind technology that will transform transportation. To do so successfully, we must design for everyone in our cities and on our roads. We believe in building a great place to work through a progressive, global culture that is diverse, inclusive, and ensures people feel valued at every level of the organization. Diversity helps us to see the world differently; it's not only good for our business, it's the right thing to do. 
Scale up, not starting up.
Our team is behind some of the industry's largest leaps forward, including the first fully-autonomous cross-country drive in the U.S, the launch of the world's first robotaxi pilot, and operation of the world's longest-standing public robotaxi fleet. We're driven to scale; we're moving towards commercialization of our technology, and we need team members who are ready to embrace change and challenges.
Formed as a joint venture between Hyundai Motor Group and Aptiv, Motional is fundamentally changing how people move through their lives. Headquartered in Boston, Motional has operations in the U.S and Asia. For more information, visit <a href="http://www.Motional.com" target="_blank">www.Motional.com</a> and follow us on Twitter, LinkedIn, Instagram and YouTube.
Motional AD Inc. is an EOE. We celebrate diversity and are committed to creating an inclusive environment for all employees. To comply with Federal Law, we participate in E-Verify. All newly-hired employees are queried through this electronic system established by the DHS and the SSA to verify their identity and employment eligibility.

2026 Summer Intern - MS/PhD - Behaviors

<h3>Job Description</h3>
Job Description
Title: Contract Research Associate/Sr. Research Associate, In-Vivo Pharmacology
Hourly Rate: $35-$55/hour
Term: 6 Month Contract 
Location: Downtown Boston (On-Site Daily)
JOB SUMMARY:
We are seeking a highly motivated research associate to join our dynamic drug discovery team. This candidate will serve a critical role in executing in vivo pharmacokinectic (PK)/pharmacodynamic (PD)/efficacy studies in mouse tumor models for projects in early discovery to the pre-IND stage. This individual will also work seamlessly with various biology functions to develop and run PD assays in the lab. This position is ideal for a talented, highly motivated and results driven individual who will thrive in a fast-paced, innovative, start-up environment.
KEY RESPONSIBILITIES:
<ul>
<li>Conduct in vivo studies by providing dosing support and executing PK/PD/efficacy studies in mouse tumor models</li>
<li>Maintain high-quality, detailed experimental records within the ELN</li>
<li>Use organizational and communication skills to effectively collaborate with colleagues across pharmacology and biology</li>
<li>May require occasional weekend oversight of experiments </li>
</ul>
PROFESSIONAL EXPERIENCE/QUALIFICATIONS
<ul>
<li>BS in Biology or a related field</li>
<li>A minimum of 2 year of relevant laboratory experience in industry</li>
<li>Skilled in animal handling, tumor implant, dosing (PO/IV/SC/IP) and necropsy techniques</li>
<li>Outstanding organizational, analytical and interpersonal skills</li>
<li>Experienced with pipetting and cell culture</li>
<li>Understanding of molecular biology techniques such as western blotting, qPCR and other plate-based assays and desire to learn to perform these assays</li>
<li>Proficiency analyzing data with excel, prism and experience using an ELN system</li>
<li>Experience with StudyLog software is a plus</li>
<li>Experience with models of autoimmunity/inflammation is a plus</li>
<li>Ability to multi-task in a fast-paced environment while maintaining the highest quality of experimental execution/quality</li>
<li>Desire to contribute to teams working on challenging technical and scientific problems</li>
</ul>

Contract Research Associate/Sr. Research Associate, In-Vivo Pharmacology (Must Have PO Dosing Experi

<h3>Job Description</h3>
Job Description
908 Devices Inc. (NASDAQ: MASS) is revolutionizing chemical analysis with its simple handheld devices, addressing life-altering applications. The Company's devices are used at the point-of-need to interrogate unknown and invisible materials and provide quick, actionable answers in vital health, safety and defense tech applications, addressing the fentanyl and illicit drug crisis, toxic carcinogen exposure, and global security threats. The Company designs and manufactures innovative products that bring together the power of complementary analytical technologies, software automation, and machine learning. For more information, visit 908devices.com
908 Devices has a corporate office in Burlington, MA with a manufacturing center in Danbury, Connecticut and a growing population of remote staff worldwide.
Position Summary
The Forensic Chemist II supports the 908 Devices' portfolio of field-portable chemical detection and identification devices. The position remotely supports the efforts of law enforcement, emergency responders, and R&amp;D partners through spectral review of analytical data from fielded users on high pressure mass spectrometers, FTIR, and Raman devices. The Forensic Chemist II position further partners with R&amp;D, Product Management to monitor emerging trends in controlled substance analysis, explosives, hazardous materials, and other relevant industries to identify essential library additions. The Forensic Chemist is an advocate for customer needs, analytical best practices, and scientific integrity in the management of the development process.
Key Responsibilities
<ul>
<li>Review customer handheld data to provide preliminary analysis and further guidance</li>
<li>Recognize when additional verification testing or analysis is needed prior to submitting results to customers</li>
<li>Investigate and troubleshoot results that appear to be anomalies or out of trend</li>
<li>Ability to make keen observations on process anomalies, recommend process improvements, and articulate findings.</li>
<li>Incorporate subject matter expertise into data interpretation, and recognize potential false-positives, and when additional verification testing or analysis is needed prior to submitting results to customers</li>
<li>Respond by phone/email/chat to client inquiries related to difficulties, questions or data review</li>
<li>Provide verbal and written reports for data analyzed in a timely manner</li>
<li>Observe and document trends in data analysis and report findings</li>
<li>Partner with other team members to develop and improve processes for service and logistics</li>
<li>Work with our Field Forensic Applications team to enhance overall customer experience</li>
<li>Collaborate with the larger forensic science community through conferences, and customer interactions</li>
<li>Participate in the onboarding and training of new analysts</li>
<li>Observe and document emerging drug trends worldwide, order and test chemical standards as necessary, and create reference spectra for library addition</li>
</ul>
 Skills &amp; Qualifications:
<ul>
<li>Exposure to chemical instrumentation, and the interpretation of said data. Examples include mass spectrometry, Raman, FTIR, and NMR.</li>
<li>Knowledge of the chemistry of drugs, explosives, pesticides, industrial toxins.</li>
<li>Concise communication of scientific information in both oral and written formats to technical and non-technical audiences.</li>
<li>The ability to engage with customers from a variety of backgrounds and experiences.</li>
<li>Understanding of the importance of standard operating procedures (SOPs) as it pertains to forensic science.</li>
<li>Previous hands-on time with portable analytical systems.</li>
<li>Hazmat, CBRNE or forensics familiarity or direct experience.</li>
<li>Experience in some customer service areas (retail, restaurant).</li>
<li>Ability to think critically and demonstrate troubleshooting/problem solving skills</li>
<li>Analytical skills to resolve problems that require the use of basic scientific, mathematical, or technical principles.</li>
<li>Ability to pay close attention to detail to carefully follow analytical procedures without losing sight of the bigger picture.</li>
<li>Ability to articulate findings to multidisciplinary teams and customers with a variety of backgrounds in a manner that is thorough and easy to understand.</li>
</ul>
Education &amp; Experience:
<ul>
<li>Master's Degree in: Chemistry, Forensic Science or similar concentrations or
<ul>
<li>Bachelor's Degree in: Chemistry, Forensic Science or similar concentrations with 2 years of experience in a laboratory setting</li>
</ul>
</li>
</ul>
We are proud to be a company changing the status quo in our industry. Join us and work with curious and innovative people, creative problem solvers, risk-takers, and dedicated colleagues as we reimagine the future of Mass Spec.
908 Devices does not discriminate in employment based on race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factors.

863 Science Jobs