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<h3>Job Description</h3>
Job DescriptionDescription:
Under the supervision of the Principal Investigator and other TFI Leadership, the Senior Research Assistant assists with the implementation of Behavioral Science research studied. This position is grant-funded and is dependent on the availability of continued grant support. It is possible that the employee’s effort will be transitioned, in whole or in part, to other research studies as needed to remain fully funded. 
This position may require a flexible working schedule with some evening and weekend hours. 
 
Responsibilities:
Implements recruitment efforts that lead to study participation
<ul>
<li> Implements and evaluates study recruitment plan by identifying and establishing recruitment sources</li>
<li>Recruits and interviews potential participants as specified by study protocols</li>
<li>Maintains and updates related databases</li>
<li>Presents about studies at community events, CAB meetings, and other appropriate forums</li>
<li>Acts as first point of contact for study inquiries and interested participants</li>
<li>Coordinate BSRP social media strategies by liaising with the communications team to post content promoting BSRP studies and to evaluate the impact of content</li>
</ul>
Coordinates study retention efforts
<ul>
<li>Implements retention efforts under the direction of the Principle Investigator and Project Manager.</li>
<li>Assists with the establishment, revision, and evaluation of retention plans</li>
<li>Completes the day-to-day tasks of study-related retention</li>
</ul>
Assists in the development of research projects and publications
<ul>
<li>Utilizes library and electronic databases to locate and obtain research articles </li>
<li>Performs administrative duties, as needed, in the development of research proposals</li>
<li>Participates in conference calls and meetings with collaborators</li>
<li>Provides updates on recruitment activities</li>
<li>Assists with the publication of research findings through editing, writing, and preparing results. </li>
<li>Assists with preparing research findings in poster or presentation format (use of Microsoft Power-Point or relevant software)</li>
<li>Develops and maintains databases and other data collection systems</li>
<li>Develops and revises study materials including study protocol, informed consent, eligibility screener, recruitment materials, and other study documents as needed</li>
<li>Prepares materials for IRB submission, liaising with Fenway compliance manager and staff to meet IRB deadlines and ensure that submissions are in line with Fenway procedures</li>
<li>Monitors the quality of written and computerized data, including regular data quality assessments (QA and QC activities)</li>
</ul>
Training
<ul>
<li>Conducts and supports training for study team members as assigned.</li>
<li>Conducts interviews and arranges study visits with study participants as specified by study protocols</li>
<li>Arranges, coordinates and oversees appointments with clients; assesses and documents eligibility and participation status of candidates; arranges follow-up appointments</li>
<li>Conducts research screenings with potential study participants in a clear, open-minded, non-judgmental context; maintains established guidelines of confidentiality and ethical accountability in all discourse with all study participants</li>
<li>Obtains initial and ongoing informed consent from study participants</li>
</ul>
Utilizes written and verbal communication to contribute to the effective functioning of research projects
<ul>
<li>Maintains current knowledge of HIV, CBT, LGBT, substance use, and trauma research by reading academic journals, articles and other relevant publications, attending conferences, seminars, forums, trainings and other presentations pertinent to the field</li>
<li>Participates in open communication and discussion among co-workers regarding changes in protocol procedure and other information pertinent to department goals and objectives</li>
</ul>
Meets Agency Participatory Expectations
<ul>
<li>Adheres to all agency and departmental policies and procedures</li>
<li>Participates in quality assessment and improvement activities as requested</li>
<li>Adheres to the highest principles of patient and client confidentiality</li>
<li>Adheres to established safety policies, procedures and precautions; identifies potential or actual unsafe situations in the environment and takes measures to rectify the situation</li>
<li>Attends all required meetings, in-services and professional trainings</li>
<li>Attends all regularly scheduled research meetings, trainings, forums and pertinent FH staff meetings</li>
<li>Maintains professional competence necessary to perform job responsibilities; maintains and provides agency with records of continuing education activities</li>
<li>Serves on agency committees and in professional organizations when requested</li>
</ul>
Performs other related duties as required
Requirements:
<ul>
<li>Bachelor’s degree in social science research or related field required </li>
<li>College-level course-work in research-design or statistics for behavioral or social sciences.</li>
<li>Ability to work harmoniously and effectively with colleagues, patients, clients and vendors across the spectrum of diversity, including but not limited to race, ethnicity, color, gender identity, sexual orientation, age, socio-economic status, national origin and immigrant status, religious or spiritual identity, disability (physical, mental, emotional and developmental), veteran status, and/or limited English proficiency. </li>
<li>Willingness to contribute towards Fenway’s efforts in becoming an anti-racist organization and promoting a culture dedicated to ongoing development in service of humility, equity, diversity, inclusion, and belonging, where differences are acknowledged and valued. </li>
</ul>
Preferred Qualifications
<ul>
<li>Demonstrated ability to take responsibility for assignments and deadlines and to work as part of a team</li>
<li>Excellent communication (written and verbal) skills and experience working with diverse communities at risk for HIV infection, particularly gay/lesbian, African American and Latino </li>
<li>Computer (Microsoft Word, PowerPoint, Email) Skills</li>
<li>Familiarity with database software (SPSS, R, Microsoft Excel)</li>
<li>Experience with data collection and analysis</li>
<li>Ability to work harmoniously with diverse groups of individuals </li>
<li>Ability to handle multiple tasks, prioritize assigned duties </li>
</ul>
 
This is a union position in a Fenway Health bargaining unit represented by 1199 SEIU United Healthcare Workers East. We offer competitive salaries, and for those who qualify, an excellent benefits package; including comprehensive medical and dental insurance plans, and a retirement plan with employer match. We also provide 11 paid holidays, paid vacation, and more.LGBTQIA+ identified persons, Black, Indigenous, and other people of color (BIPOC), and individuals from other historically underrepresented communities are strongly encouraged to apply.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionOur mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized benefit to society. We're developing a mammalian synthetic biology platform––from cells to software––to enable the design and manufacture of next-generation therapeutics. We are seeking a Senior Associate Scientist, Viral Vector to join our Cell Line Development team in Boston, MA. The ideal candidate will have a proven track record performing lentiviral vector stable packaging or producer cell line development in an industry setting. They will be a key contributor to our team, participating in the creation of stable producer cell lines for lentiviral vector therapeutics and research projects to improve our cell line development workflows. They will also work closely with Asimov’s synthetic biology and process development teams. This is a unique opportunity to work at a nimble, forward-thinking synthetic biology startup and help build the future of biological engineering.About the Role:
<ul>
<li>Perform lentiviral vector stable producer cell line development processes including transfection, pool generation, single cell cloning, characterization, and cell banking using state-of-the-art equipment.&nbsp;</li>
<li>Perform assays to assess quantity, potency and infectivity of lentiviral vector preparations.</li>
<li>Support innovation through development of novel workflows and applications</li>
<li>Support research projects to develop viral vector production methods to enhance product quality attributes such as empty/full ratio, potency and/or cell targeting.</li>
<li>Work effectively as part of a cross-functional team in support of a Lentiviral CLD platform and in collaboration with Synthetic Biology and Process Development teams.</li>
<li>Design experiments, analyze data, troubleshoot, and maintain detailed records.&nbsp;</li>
<li>Represent LV CLD on project teams, making decisions for cell line development activities and effectively communicating results, progress and plans.</li>
</ul>
About You:
<ul>
<li>B.S or M.S. in Biological Engineering, Virology, Cell Biology, Molecular Biology, or a related field.</li>
<li>5+ years of hands-on experience in biopharma with a minimum of 3 years focused on lentiviral vector producer cell line development in support of GLP or GMP production of cell or gene therapies.</li>
<li>Extensive experience performing viral transductions, flow cytometry, and quantitative gene expression analyses (ddPCR or qPCR).&nbsp;</li>
<li>Experience with downstream purification of lentiviral vectors, T-cell transduction assay, viral genome engineering, and/or host cell genome engineering related to virus production or producer cell line technologies is highly desired.</li>
<li>Comfortable working with large, multidimensional datasets and applying statistical or computational methods to extract actionable biological or process insights.</li>
<li>Strong written and verbal communication skills required.</li>
</ul>
We're fueled by a vision to transform biological engineering into a fully-fledged engineering discipline. Should you join our team, you will grow with a constantly evolving organization and push the frontiers of synthetic biology. Company culture is key to Asimov, and ours is a culture of recombination; we believe that our mission can only be achieved by bringing together a diverse team with a mixture of backgrounds and perspectives.

Senior Associate Scientist, Viral Vector Cell Line Development

<h3>Job Description</h3>
Job DescriptionDescription:Work Location: Hybrid (remote and in-person work expected in Boston, MA area)Expected Schedule: 15 hours a week within a usual Monday-Friday, first shift schedule. May require occasional flexible working schedule with some evening and weekend hours.
 
Function
This position sits within The Fenway Institute (TFI), the research, education, and policy department of Fenway Health. Reporting to the Assoc. Director of Research Operations and under the supervision of the Principal Investigator, and other TFI Leadership, the Research Associate supports the implementation of research studies. 
 
Position Funding
This position is grant-funded and is dependent on the availability of continued grant support for the assigned study/studies. It is possible that the employees’ effort will be transitioned, in whole or in part, to other research studies as needed.
 
Representative Duties
 
Study Preparation and Administrative/Outreach Implementation
<ul>
<li>Assist with study startup: Help prepare study documents (e.g., protocols, consent forms, case report forms, participant files, regulatory binders, and visit checklists).</li>
<li>Regulatory compliance: Ensure studies meet regulatory requirements (e.g., IRB submissions, informed consent documentation).</li>
<li>Participant recruitment: Implement study recruitment efforts that lead to study participation, with responsibilities such as reviewing records, identifying and establishing recruitment opportunities and initiating outreach to prospective research participants, attending community events; creating recruitment materials; and maintaining recruitment and screening calendars, databases, and study documentation. </li>
</ul>
 
Participant Interaction and Data Collection
<ul>
<li>Obtain informed consent: Explain study procedures and risks/benefits to participants. </li>
<li>Conduct study visits: Schedule study visits and maintain study calendar/visit spreadsheets. Confirm participant eligibility and assist with or perform tasks like administering surveys, scheduling follow-ups, and accurately and comprehensively completing visit notes, data collection instruments, case report forms, etc.</li>
<li>Monitor participant safety: Report non-compliance, adverse events, or unanticipated problems promptly to the research leads.</li>
</ul>
 
Data Management and Documentation
<ul>
<li>Maintain accurate records: Ensure timely and accurate entry of data into study files, including paper files and electronic databases (e.g., REDCap, EDC systems), and keep organized and complete source document files, including signed consent forms, case report forms, and lab reports.</li>
<li>Assist in data cleaning and audit preparation: Monitor the quality of collected data through routine and ad hoc quality assurance and quality improvement activities (e.g., record review, monitor visit preparation, completion of visit checklists) and respond to data queries.</li>
<li>Use best research practices, as defined by Good Clinical Practice (GCP), TFI standard operating procedures, study specific procedures, and the research protocol and follow all established guidelines of confidentiality and ethical accountability. </li>
</ul>
 
Communication and Collaboration
<ul>
<li>Liaise with internal and external teams: Communicate with investigators, sponsors, IRBs, and study monitors. Share study information to Fenway Health staff, patients, and community.</li>
<li>Attend team and departmental meetings: Provide updates and help resolve logistical or compliance issues.</li>
<li>Support training and onboarding: Help train new research assistants or interns on study protocols and procedures</li>
</ul>
 
Administrative and Logistical Support
<ul>
<li>Manage supplies and equipment: Track, maintain, and order study-specific materials.</li>
<li>Schedule appointments and organize calendars: Coordinate participant visits and team availability.</li>
<li>Assist with study closeout: Ensure all documents are archived according to protocol and regulatory guidelines.</li>
<li>Assist in the development of research projects and publication/dissemination of study findings: Utilize library and electronic databases to locate and obtain research articles and performs administrative duties, as needed, in the development of research proposals or manuscripts.</li>
<li>Develop and share understanding of research context: Monitor and track institutional, state level and federal level policies impacting participant population and research; develop knowledge of field by completing pertinent trainings, attending didactics, reading academic journals, articles and other relevant publications, attending conferences, seminars, forums, trainings and other presentations.</li>
</ul>
 
Other related duties as required.
 
Meets Agency Participatory Expectations 
<ul>
<li>Adheres to all agency and departmental policies and procedures</li>
<li>Identifies potential or actual unsafe situations in the environment and takes measures to rectify the situation</li>
<li>Attends all required meetings, in-services and professional trainings</li>
<li>Maintains professional competence necessary to perform job responsibilities; maintains and provides agency with records of continuing education activities</li>
<li>Serves on agency committees and in professional organizations when requested</li>
<li>Work harmoniously and effectively with colleagues, patients, clients and vendors across the spectrum of diversity, including but not limited to race, ethnicity, color, gender identity, sexual orientation, age, socio-economic status, national origin and immigrant status, religious or spiritual identity, disability (physical, mental, emotional and developmental), veteran status, and/or limited English proficiency.</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s degree or higher in field related to social science research. </li>
<li>Excellent communication (written and verbal) skills and experience working with diverse communities at risk for HIV infection, particularly sexual minority men, transgender individuals, and BIPOC individuals.</li>
<li>Ability to work harmoniously and effectively with colleagues, patients, clients and vendors across the spectrum of diversity, including but not limited to race, ethnicity, color, gender identity, sexual orientation, age, socio-economic status, national origin and immigrant status, religious or spiritual identity, disability (physical, mental, emotional and developmental), veteran status, and/or limited English proficiency.</li>
<li>Willingness to contribute towards Fenway’s efforts in becoming an anti-racist organization and promoting a culture dedicated to ongoing development in service of humility, equity, diversity, inclusion, and belonging, where differences are acknowledged and valued.</li>
</ul>
Preferred Qualifications
<ul>
<li>Demonstrated ability to take responsibility for assignments and deadlines and to work as part of a team</li>
<li>1-2 years human subjects research experience</li>
<li>Detail-oriented</li>
<li>Computer (Microsoft Word, Power-Point, Email) Skills</li>
<li>Familiarity with database software (SPSS, Microsoft Excel)</li>
</ul>
 
 This is a union position in a Fenway Health bargaining unit represented by 1199 SEIU United Healthcare Workers East. We offer competitive salaries, and for those who qualify, an excellent benefits package; including comprehensive medical and dental insurance plans, and a retirement plan with employer match. We also provide 11 paid holidays, paid vacation, and more.LGBTQIA+ identified persons, Black, Indigenous, and other people of color (BIPOC), and individuals from other historically underrepresented communities are strongly encouraged to apply.

Research Associate

<h3>Job Description</h3>
Job Description
Are you detail-oriented and passionate about maintaining high-quality standards in a fast-paced environment? We're looking for a fill-time Post Processing Technician I to join our team in the Processing Department. Available shifts include Monday through Friday 7:30AM - 4:00PM or Friday through Monday 7:00AM - 5:30PM. This position plays a vital role in supporting the post-processing process, ensuring compliance, and maintaining product quality from start to finish. If you're excited to work with a dedicated team in a dynamic setting, this could be the perfect opportunity for you!
As a Post Processing Technician I, you will be responsible for performing routine tasks across all processing areas, working under the guidance of the Processing Supervisor and Post Processing Technician III. Your responsibilities will include conducting green waste disposal processes, trimming batches by hand and machine, and assisting with the dry and cure processes. You'll play a role in maintaining quality control measures, ensuring batches meet product standards, and supporting inventory management by keeping accurate records. In addition, you will be expected to keep your workspaces and machinery clean, sanitized, and organized to maintain operational efficiency.
Previous experience is preferred but not required. The ideal candidate will have a keen eye for detail and the ability to focus on sensitive and complex tasks. Strong verbal and written communication skills, flexibility, and adaptability are essential to succeed in this role. You must be able to stand for extended periods, lift up to 50 lbs occasionally, and perform manual tasks requiring fine motor skills. Safety is a priority, and you will be required to maintain balance while using ladders or performing tasks such as stooping, kneeling, or reaching.
If you're ready to be part of a supportive team in an evolving environment and are excited about contributing to our post-processing process, we encourage you to apply today!

Post Processing Technician 1

<h3>Job Description</h3>
Job Description
Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA)&nbsp;
We are seeking a Research Scientist– Oncology Translational Research for a global pharmaceutical client. You will join the Translational Research team within the Oncology Thematic Research Center in Cambridge, MA. You will work broadly with the research organization to support drug discovery programs, by conducting experimental work in a translational setting, including developing and implementing cutting-edge technology and novel cellular, molecular, and biochemical assays in cancer research and deliver data for Oncology TRC programs.&nbsp;
This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Cambridge, MA&nbsp;
Work hours/schedule: M - F, typical work hours are 9:00am to 5:00pm&nbsp; Parking Fee: Candidates must be agreeable with the $20/day parking fee at Cambridge Crossings.&nbsp;
This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.&nbsp;
Responsibilities:&nbsp;&nbsp;
<ul>
<li>
Design, optimize, and set up high-throughput screening cellular assays to characterize drug responses and combinations in various in vitro oncology models.&nbsp;
</li>
</ul>
<ul>
<li>
Conduct molecular, biochemical and related assays including qPCR, ELISA, Western blot, immunostaining and basic microscopy.&nbsp;
</li>
</ul>
<ul>
<li>
Develop biomarker, pharmacodynamic and target engagement assays.&nbsp;
</li>
</ul>
<ul>
<li>
Execute, troubleshoot and interpret scientific experiments with some supervision.&nbsp;
</li>
</ul>
<ul>
<li>
Effectively communicate and document experimental procedures, analyze results and data through study reports and internal meetings.&nbsp; &nbsp;
</li>
</ul>
Requirements:&nbsp;&nbsp;
<ul>
<li>
3+ years of experience in conducting cancer cell line and primary cell culture, expansion and functional assays.&nbsp;
</li>
</ul>
<ul>
<li>
Experienced in the design and development of cell-based and molecular assays in a high-throughput manner.&nbsp;
</li>
</ul>
<ul>
<li>
Drug combination screen&nbsp;
</li>
</ul>
<ul>
<li>
Experience performing analysis of protein and DNA/RNA samples using a variety of methodologies including but not limited to western blot, flow cytometry, qPCR, MSD/ELISA, RNAi, CRISPR.&nbsp;
</li>
</ul>
<ul>
<li>
Proficiency in utilizing software such as Graph Pad, Microsoft Office, etc. for data analysis and figure generation is required.&nbsp;
</li>
</ul>
<ul>
<li>
BS or MS Degree.&nbsp;
</li>
</ul>
Please submit your resume to our network at <a href="https://www.stage4solutions.com/careers/" target="_blank">https://www.stage4solutions.com/careers/</a> (please apply to the Research Scientist– Oncology Translational Research (Onsite – Cambridge, MA) role).&nbsp;
Please feel free to forward this project opening to others who may be interested.&nbsp;
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates’ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.&nbsp;
Compensation: $45hr. - $50.91/hr.&nbsp;
#LI-SW1&nbsp;&nbsp;&nbsp;

Research Scientist- Oncology Translational Research (Onsite - Cambridge, MA)

<h3>Job Description</h3>
Job Description
Job Title: Biologist Location: Boston, MA 02210 Work Schedule: Monday–Friday, 8:00 AM – 5:00 PM
Job Overview:
We are seeking a highly motivated Biologist to join our Downstream Process Development team. The candidate will contribute to the purification and characterization of viral vectors, biologics, or recombinant proteins, supporting process development and manufacturing activities.
Key Responsibilities:
<ul>
<li>
Execute purification processes including affinity chromatography (e.g., AVB, CaptureSelect) and ion-exchange chromatography (AEX, CEX).
</li>
<li>
Operate AKTA systems (Avant, Pure, or Pilot) for small- to large-scale purification runs.
</li>
<li>
Perform tangential flow filtration (TFF) for buffer exchange and product concentration.
</li>
<li>
Support experimental design, data collection, and documentation following GMP/GLP guidelines.
</li>
<li>
Troubleshoot and optimize purification processes.
</li>
<li>
Analyze samples using relevant methods (UV, SDS-PAGE, ddPCR, ELISA, HPLC).
</li>
<li>
Collaborate cross-functionally with upstream, analytical, and manufacturing teams.
</li>
<li>
Maintain lab equipment, buffers, column inventory, and compliance with safety standards.
</li>
</ul>
Qualifications:
Education:
<ul>
<li>
Master’s degree in Biochemistry, Chemical Engineering, Biotechnology, or related field.
</li>
</ul>
Experience:
<ul>
<li>
Minimum 2 years of hands-on purification experience in academic or industry settings.
</li>
</ul>
Technical Skills:
<ul>
<li>
Strong experience with ion-exchange and affinity chromatography.
</li>
<li>
Familiarity with buffer preparation.
</li>
<li>
Knowledge of basic analytical methods for product characterization.
</li>
</ul>
Soft Skills:
<ul>
<li>
Strong attention to detail and excellent documentation habits.
</li>
<li>
Effective communication and teamwork skills.
</li>
<li>
Ability to manage multiple tasks and meet project timelines.
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Experience in AAV or other viral vector purification.
</li>
<li>
Experience with AKTA systems and Unicorn software.
</li>
</ul>

Purification Scientist - Biologics / Viral Vectors

<h3>Job Description</h3>
Job DescriptionSalary: 
Description: 
We are seeking an experienced Quality Control Microbiologist to join Marianas Technical Operations organization, advancing personalized medicine and radiopharmaceuticals. This person will be responsible for routine microbiological testing including environmental monitoring, environmental monitoring performance qualifications, growth promotion, bioburden, endotoxin, and sterility testing to support product release. In addition to supporting routine testing, this role will ensure that work is completed with SOPs and adheres to strict quality standards.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Perform environmental monitoring and environmental monitoring performance qualifications (viable, non-viable, and surface monitoring) of classified areas and maintain database of recovered data and isolates to actively trend EM data.</li>
<li>Perform bioburden, endotoxin, and sterility testing to support product release.</li>
<li>Conduct growth promotion testing and release of media.</li>
<li>Ensures aseptic operator qualification and process simulations are performed aseptically according to GMP compliance.</li>
<li>Microbial enumeration and data analysis from microbiological testing.</li>
<li>Experienced with raw material testing is considered a plus.</li>
<li>Identifying, investigating, and resolving microbial action limits, Out of Specification (OOS) results, and deviations.</li>
<li>Maintain laboratory equipment in accordance with internal procedures.</li>
<li>Adhere to SOPs to ensure high quality standards.</li>
<li>Track progress against project timelines, generate regular status updates, and communicate progress and risks to management.</li>
<li>Adhere to safe laboratory practices.</li>
<li>Multi-task across several projects and manage time effectively to achieve results.</li>
<li>Perform other duties as assigned.</li>
</ul>
Requirements/Skills:
<ul>
<li>Bachelors degree in microbiology or related field with a minimum of two years of experience working in a GMP environment in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals will be considered as a plus.</li>
<li>Experience with cGMP and GMP regulations.</li>
<li>Commitment to maintain data integrity through strict adherence to standardized procedures and relevant compliance requirements.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Comfortable handling radioactivity and follow proper ALARA (As Low As Reasonably Achievable) technique Strong communication skills, with motivation to work effectively and cooperatively with others, and to establish and maintain good working relationships.</li>
</ul>
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Quality Control Analyst II, Microbiology

<h3>Job Description</h3>
Job DescriptionSalary: $50K - $55K 
Gloucester Marine Genomics Institute (GMGI) is an exciting independent research institute addressing critical challenges facing our oceans, human health, and the environment through innovative scientific research and education. GMGI is looking for a Research Associate to join our team studying the biology of exceptionally long-lived marine animals. Our goal is to translate evolutionary insights from these exceptional animals into interventions that promote human healthspan and combat age-related diseases, using zebrafish as a development platform. This position will conduct zebrafish genetics work and husbandry, testing these evolutionary targets to extend healthy functionality. This project will use modern genetic editing techniques and apply new assays to modulate and test the molecular mechanisms of aging.
The ideal candidate will have experience with aquatic husbandry, standard molecular biology techniques, excellent communication skills, attention to detail, and the ability to work with a multi-disciplinary team of collaborators. This is an extraordinary opportunity for a dynamic and motivated individual to learn a powerful genetic model and to advance aging research in an entrepreneurial and exciting work environment.
 
Responsibilities:
<ul>
<li>Standard molecular biology and genetics experimental research.</li>
<li>Contribute to the maintenance of the aquatic facility, including feeding, water quality, and health monitoring.</li>
<li>Contribute to the generation and maintenance of transgenic zebrafish lines, including microinjection, mutant screening, and genotyping.</li>
<li>Apply assays to quantify biological aging in zebrafish, including taking tissue samples, performing histology, and compound neuro-muscular functionality.</li>
<li>Maintain a comprehensive electronic lab notebook.</li>
<li>Contribute to grant proposals and publications, and present results at lab meetings and other venues.</li>
<li>Participate in institutional fund-raising activities and community outreach activities.</li>
</ul>
 
Qualifications:
<ul>
<li>BS or MS in genetics, molecular or cell biology, or related field, with lab experience.</li>
<li>Experience with standard molecular biology techniques such as DNA/RNA isolation, PCR/qPCR, molecular cloning, and CRISPR gene editing.</li>
<li>Experience with the husbandry of aquatic models.</li>
<li>Experience with zebrafish and histology is desirable.</li>
<li>Ability to work independently to design and execute experiments</li>
<li>Strong data analysis skills using standard bioinformatic and statistic software packages</li>
<li>Attention to detail and strong problem-solving skills</li>
<li>Excellent organization skills and the ability to multi-task in a fast-paced environment</li>
<li>Excellent communication and teamwork skills.</li>
<li>Enthusiasm and commitment to GMGIs mission for science and education.</li>
</ul>
This position will report to the Research Scientist.
 
It's our goal as an employer to provide an enriching and supportive environment for our employees. We are proud to offer a benefit package that includes:
Health and Dental Insurance
Medical and Dependent Flex Spending Accounts
Long Term Disability
Life Insurance
Paid Time Off
403(b) Retirement Plan
12 Paid Holidays
Applicants must be authorized to work in the US.
 
About GMGI 
Gloucester Marine Genomics Institute (GMGI) was launched in 2013 in the belief that the ocean represents a new source of opportunity. As a not-for-profit whose ambitious mission is to address critical challenges facing our oceans, human health and the environment through innovative scientific research and education GMGI is demonstrating that there is vast potential in marine science discovery powered by genomics.
GMGI is proud to be an equal opportunity employer, and all aspects of employment are based on merit, competence, performance and business need.
In addition to researching diversity in our oceans, GMGI is committed to supporting diversity in our workforce and classrooms. We know that having varied backgrounds and experiences stimulates discussion and new ideas. We are committed to taking action on diversity, equity, and inclusion through providing substantial training opportunities to increase our self-awareness as an organization and building a team of staff and students from uniquely different backgrounds. Please visit our website for more information: <a href="http://www.gmgi.org" target="_blank">www.gmgi.org</a>

Research Associate I - Marine Biomedical Discovery

<h3>Job Description</h3>
Job DescriptionSalary: 
JOB SUMMARY
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development.
 
PRIMARY DUTIES AND RESPONSIBILITIES
<ul>
<li>Prepares and analyzes products to determine chemical and physical properties.</li>
<li>Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed.</li>
<li>Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports.</li>
<li>Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks.</li>
<li>Performs data generation, analysis and more complicated problem solving with a minimal rework.</li>
<li>Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting.</li>
<li>Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration.</li>
<li>Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies.</li>
<li>Performs system maintenance and calibrations to ensure equipment is operating with specified requirements.</li>
<li>Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules.</li>
<li>Documents work in a clear and organized manner.</li>
<li>Follows all safety rules and regulations and conducts periodic safety audits.</li>
<li>Follows all cGMP rules and regulations.</li>
</ul>
REQUIREMENTS &amp; QUALIFICATIONS
Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required.
 
MINIMUM SKILLS REQUIREMENTS
<ul>
<li>Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently.</li>
<li>A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel.</li>
<li>Must have excellent organizational, verbal communication and technical documentation skills.</li>
<li>Solid computer skills.</li>
<li>Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples.</li>
<li>Must be a team player with integrity and concern for the quality of Company products, services and staff members.</li>
</ul>

Chemist II

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Principal Scientist, CMC Radiochemistry
Description:
We are seeking an experienced Scientist I/II, CMC Radiochemistry to join Mariana Oncology's CMC organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for radiochemistry development through validations of pipeline projects leading to and enabling production, development, and advancement of radiotherapeutics and nuclear imaging probes. You will join the development efforts in support of the next generation radiotherapeutics for Mariana Oncology's clinical trial programs.
Illustrative Breadth of Responsibilities:
<ul>
<li>Radiolabeling/ coordination chemistry process, analytical development and troubleshooting with a broad range of radioisotopes, including but not limited to: Lu-177, Ac-225, Zr-89, Cu-64, In-111, Ga-68 and Pb-212.</li>
<li>Early formulation development, process and analytical method optimization to ensure drug product stability.</li>
<li>Participate in the development and process validation of radiopharmaceutical productionprocedures for use in preclinical and clinical studies.</li>
<li>Support CMC drafting and executing Master Batch Records, protocols for validation of manufacturing processes of radiopharmaceuticals, validation of analytical methods.</li>
<li>Participate and support CMC analytical development, method validation, and reporting activities, including but not limited to Identity, Purity, Impurities and Assays.</li>
<li>Support CMC in preparation of method validation protocols, execution of method validations, and authoring/review of reports, SOPs, and other technical documents for technical correctness, quality, and regulatory compliance.</li>
<li>Perform analysis, tabulating and gathering data for CMC sections (Module 3), development reports for IND and IMPD, to regulatory agencies including FDA and EMEA.</li>
<li>Support team communications in disseminating results, which may come in the form of presentations or reports.</li>
<li>Contribute to the organization and maintenance of the laboratory.</li>
</ul>
Requirements/Skills:
<ul>
<li>A Ph.D. in Inorganic Chemistry, Organic Chemistry, Radiochemistry, or related discipline and 0+ years of Biotech or Pharmaceutical industry experience; BS or MS in Chemistry or related discipline and 4 6+ years of Biotech or Pharmaceutical industry experience.</li>
<li>Radiopharmaceutical drug substance and drug product development experience is a plus.</li>
<li>Development experience for the biologics and peptides GMP manufacturing is a plus.</li>
<li>A strong background and in-depth working knowledge of biologics and peptides andconjugates analysis, including but not limited to: Assay and Purity (RP-HPLC, IP-RP-HPLC,AEX/CEX-HPLC), with LC-MS and LC-ICP-MS experience being a plus.</li>
<li>Knowledgeable in regulatory requirements and guidelines (cGMP, ICH, FDA, and USP, EP) with the ability to apply to the Phase appropriate pharmaceutical development. GMP pharmaceuticals validation experience is a plus.</li>
<li>Experience with regulatory documentation is preferred. </li>
<li>Understanding of chemistry manufacturing and controls (CMC) documentation for novelcompounds consistent with requirements for IND, NDA, or other regulatory pathways.</li>
<li>Good understanding of the radiation safety regulations and guidelines is preferred.</li>
<li>Strict adherence to data integrity is required. </li>
<li>Proven ability to adhere to good documentation standards and maintain detailed records of all work performed.</li>
<li>Excellent verbal and written communication skills.</li>
</ul>
Mariana Oncologys Values
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

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