ZipRecruiter

Log In

1

In Vivo Study Manager Jobs (NOW HIRING)

Astrix Inc

Scientist II - In Vivo

Ridgefield, CT · On-site

$40 - $42/hr

This role involves independently designing and executing in vivo studies, analyzing experimental outcomes, and contributing to the advancement of drug discovery programs. The ideal candidate will ...

Amgen

Senior Associate (In Vivo)

Thousand Oaks, CA

Study data acquisition, organization, analysis, quality control * Graphing and PP deck preparation for presentation * Study/data documentation * Study sample processing/inventory/tracking What we ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA

$80K - $100K/yr

The In Vivo Operations specialist will also function as a study manager assisting the study directors. The In vivo operations specialist will be a key member of the Pharmaron Operations Team and ...

RPM ReSearch

Study Director II

Corpus Christi, TX

$80K - $110K/yr

... in-vivo study execution or direction, preferably in pharmacology, pharmacokinetics, or toxicology. * Experience managing NHP studies is highly preferred. * Strong communication and organizational ...

Amgen, Inc.

Senior Associate (In Vivo)

Thousand Oaks, CA · On-site

$15.75 - $19/hr

Study data acquisition, organization, analysis, quality control * Graphing and PP deck preparation for presentation * Study/data documentation * Study sample processing/inventory/tracking What we ...

Pharmaron

In Vivo Operations Specialist

Carlsbad, CA · On-site

$80K - $100K/yr

The In Vivo Operations specialist will also function as a study manager assisting the study directors. The In vivo operations specialist will be a key member of the Pharmaron Operations Team and ...

next page

Showing results 1-20

All JobsIn Vivo Study JobsIn Vivo Study Manager Jobs

In Vivo Study Manager information

What are some common challenges faced by In Vivo Study Managers, and how can they be addressed?

In Vivo Study Managers often encounter challenges such as coordinating complex study timelines, ensuring regulatory compliance, and managing cross-functional teams. Balancing the demands of multiple studies while maintaining high standards for animal welfare and data integrity can also be demanding. Effective communication, strong organizational skills, and proactive problem-solving are essential for overcoming these challenges. Establishing clear protocols and fostering collaboration between research, veterinary, and regulatory teams can help streamline operations and ensure successful study outcomes.

What are the key skills and qualifications needed to thrive as an In Vivo Study Manager, and why are they important?

To thrive as an In Vivo Study Manager, you need a solid background in animal science, pharmacology, or related biological sciences, typically supported by a relevant degree and experience in preclinical research. Familiarity with laboratory animal management systems, regulatory compliance tools (such as GLP), and data analysis software is essential. Strong organizational skills, attention to detail, leadership, and effective communication are standout soft skills for coordinating study teams and reporting results. These competencies are crucial for ensuring ethical, efficient, and high-quality execution of in vivo studies in compliance with regulatory standards.

What is the difference between In Vivo Study Manager vs In Vivo Study Coordinator?

AspectIn Vivo Study ManagerIn Vivo Study Coordinator
ResponsibilitiesOversees entire in vivo studies, manages teams, ensures protocol complianceAssists with daily study tasks, prepares materials, supports study execution
Required CredentialsBachelor's or higher in life sciences, experience in study managementRelevant degree, experience in laboratory or clinical settings
Work EnvironmentResearch labs, clinical facilities, project management settingsLaboratories, research facilities, clinical trial sites
Industry UsageCommonly used in pharmaceutical, biotech, and research organizationsOften found in similar settings, supporting study teams

The In Vivo Study Manager typically leads and oversees entire studies, requiring more experience and management skills. The In Vivo Study Coordinator supports daily operations and assists managers, focusing on execution rather than leadership. Both roles are essential in research settings, but the manager has broader responsibilities and higher qualifications.

What does an In Vivo Study Manager do?

An In Vivo Study Manager is responsible for planning, overseeing, and coordinating research studies that involve live animal models to evaluate the efficacy, safety, and pharmacology of new drugs or treatments. They ensure that all experiments comply with regulatory guidelines and ethical standards, manage study timelines and budgets, and supervise laboratory staff. Additionally, they analyze study data, prepare reports, and communicate findings to project teams or regulatory bodies.
Infographic showing various In Vivo Study Manager job openings in the United States as of May 2026, with employment types broken down into 11% Locum Tenens, 25% Full Time, 56% Part Time, 4% Contract, and 4% Nights. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.
Scientist, In Vivo Pharmacology

Scientist, In Vivo Pharmacology

Alnylam Pharmaceuticals

Cambridge, MA • On-site

$110K - $165K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Job description

Overview
We are seeking a highly motivated Scientist, In Vivo Pharmacology to support the development of innovative therapeutics for autoimmune diseases and oncology. The ideal candidate will have strong hands-on experience in preclinical in vivo models and a solid understanding of immunology and translational research.
In this role, you will design and execute in vivo studies, perform downstream ex vivo analyses, and collaborate cross-functionally (including with CRO partners) to advance drug discovery programs. In vivo models are critical for evaluating therapeutic efficacy, immune modulation, and translational relevance in both autoimmune and tumor settings
This position is onsite and will be primarily located in Cambridge, MA.
Key Responsibilities
  • Design and execute in vivo pharmacology studies in autoimmune and tumor models.
  • Perform in vivo procedures including animal dosing (IV, IP, SC, PO), tumor implantation, disease induction, and tissue collection.
  • Conduct ex vivo analyses from collected tissues, including: Flow cytometry for immune profiling, qPCR for gene expression analysis and cytokine and biomarker assessment
  • Analyze and interpret data (tumor growth, disease scores, immune readouts) and prepare clear study summaries and presentations.
  • Collaborate with internal teams and external CROs to design, execute, and monitor outsourced studies; ensure data quality and timely delivery.
  • Contribute to study design, including model selection, dosing strategies, and endpoint definition.
  • Maintain accurate documentation in compliance with regulatory and ethical standards (e.g., IACUC).

Qualifications
  • PhD, Masters, Bachelors, in Immunology, Biology, Pharmacology, or a related discipline.
  • PhD 0+, Masters 10+ years, Bachelors 12+ of hands-on experience in in vivo pharmacology within biotech or pharmaceutical settings.
  • Demonstrated expertise in autoimmune disease models and tumor models, including study design, execution, and data interpretation.
  • Proficiency in common in vivo techniques: animal handling and dosing (multiple routes), tumor implantation and measurement, disease scoring in autoimmune models, necropsy and tissue collection.
  • Experience analyzing downstream endpoints such as flow cytometry, cytokine assays, molecular biomarkers, qPCR, and ELISA assays.
  • Demonstrated ability to independently design experiments, troubleshoot, and manage multiple studies simultaneously.
  • Strong organizational skills, attention to detail, and commitment to scientific rigor and reproducibility.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate across multidisciplinary teams.

#LI-JR1
U.S. Pay Range
$110,400.00 - $165,600.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.

Apply