Study Director
$74K - $110K/yr
Join Our Team as a Study Director and Research Scientist! Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies ...
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$74K - $110K/yr
Join Our Team as a Study Director and Research Scientist! Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies ...
Quick apply
$74K - $110K/yr
Join Our Team as a Study Director and Research Scientist! Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies ...
San Diego, CA · On-site
$110K - $180K/yr
Position Summary We are seeking a hands-on Study Director with strong surgical experience in large animal models to lead and execute in vivo preclinical studies from initiation through final ...
San Diego, CA · On-site
$110K - $180K/yr
Position Summary We are seeking a hands-on Study Director with strong surgical experience in large animal models to lead and execute in vivo preclinical studies from initiation through final ...
Hercules, CA · On-site
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
Hercules, CA · On-site
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
Hercules, CA · On-site
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
Hercules, CA · On-site
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
$120K - $150K/yr
Serve as the Study Director for a variety of biocompatibility, safety, and efficacy studies for medical devices and pharmaceutical products in accordance with Good Laboratory Practice (GLP) for Non ...
Brisbane, CA · On-site +1
$245K - $260K/yr
Description At Arcus, the Director, Clinical Pharmacology (CP) functions as the Clinical ... This includes design and execution of clinical pharmacology studies, design of clinical ...
Brisbane, CA · On-site +1
$245K - $260K/yr
Description At Arcus, the Director, Clinical Pharmacology (CP) functions as the Clinical ... This includes design and execution of clinical pharmacology studies, design of clinical ...
Alameda, CA · On-site
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
Alameda, CA · On-site
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
Alameda, CA · On-site
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
Alameda, CA · On-site
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
The DMPK Director has strong scientific, technical and leadership skills to develop and implement ... Expert knowledge of in vitro and in vivo ADME studies * Strong experience of managing external DMPK ...
San Diego, CA · On-site
$140K - $185K/yr
The Associate Director Clinical Pharmacology and Pharmacokinetics will play a crucial role in our ... Design and oversee PK, PK/PD, and exposure-response analyses to support dose selection, study ...
San Diego, CA · On-site
$140K - $185K/yr
The Associate Director Clinical Pharmacology and Pharmacokinetics will play a crucial role in our ... Design and oversee PK, PK/PD, and exposure-response analyses to support dose selection, study ...
Carlsbad, CA · On-site +1
$216K - $265K/yr
Provide expert advice and guidance on IND enabling ADME and PK studies from protocol to finalized ... This position will have direct report(s) REQUIREMENTS: * Ph.D. in relevant biomedical research with ...
Carlsbad, CA · On-site +1
$216K - $265K/yr
Provide expert advice and guidance on IND enabling ADME and PK studies from protocol to finalized ... This position will have direct report(s) REQUIREMENTS: * Ph.D. in relevant biomedical research with ...
Irvine, CA · On-site +1
This is a senior leadership role responsible for endtoend oversight of complex clinical studies and ... Plan and direct complex activities with large scale or significant business impact with the ...
Irvine, CA · On-site +1
This is a senior leadership role responsible for endtoend oversight of complex clinical studies and ... Plan and direct complex activities with large scale or significant business impact with the ...
This is a senior leadership role responsible for end-to-end oversight of complex clinical studies ... Plan and direct complex activities with large scale or significant business impact with the ...
This is a senior leadership role responsible for end-to-end oversight of complex clinical studies ... Plan and direct complex activities with large scale or significant business impact with the ...
Carlsbad, CA · On-site
$216K - $265K/yr
Provide expert advice and guidance on IND enabling ADME and PK studies from protocol to finalized ... This position will have direct report(s) REQUIREMENTS: * Ph.D. in relevant biomedical research with ...
Carlsbad, CA · On-site
$216K - $265K/yr
Provide expert advice and guidance on IND enabling ADME and PK studies from protocol to finalized ... This position will have direct report(s) REQUIREMENTS: * Ph.D. in relevant biomedical research with ...
We are seeking an Associate Director, Real-World Evidence (RWE) , who will lead real-world evidence ... Lead design and oversight of observational studies (retrospective/prospective cohorts, registries ...
We are seeking an Associate Director, Real-World Evidence (RWE) , who will lead real-world evidence ... Lead design and oversight of observational studies (retrospective/prospective cohorts, registries ...
$155K - $165K/yr
... or Study Director for preclinical studies in various species. - Assisting in the preparation and review of study protocols and reports. - Contributing to activities related to the Institutional ...
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$155K - $165K/yr
... or Study Director for preclinical studies in various species. - Assisting in the preparation and review of study protocols and reports. - Contributing to activities related to the Institutional ...
Palo Alto, CA · On-site
$255K - $285K/yr
Support GLP toxicology studies, review toxicokinetic reports, and monitor regulated bioanalysis * Monitor bioanalytical method development, validation, sample analysis, and review/approve reports
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Palo Alto, CA · On-site
$255K - $285K/yr
Support GLP toxicology studies, review toxicokinetic reports, and monitor regulated bioanalysis * Monitor bioanalytical method development, validation, sample analysis, and review/approve reports
Redwood City, CA · On-site
$211K - $264K/yr
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors ...
Redwood City, CA · On-site
$211K - $264K/yr
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors ...
Research Scientist/Study Director Ocular Description: We are seeking to find an accomplished Ocular Scientist with requirements of a broad knowledge of Ocular anatomy, physiology, and biochemistry to ...
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Research Scientist/Study Director Ocular Description: We are seeking to find an accomplished Ocular Scientist with requirements of a broad knowledge of Ocular anatomy, physiology, and biochemistry to ...
We know that our success is a direct result of the exceptional talents and dedication of our ... The individual will ensure that studies are conducted with appropriate quality, GLP compliance ...
We know that our success is a direct result of the exceptional talents and dedication of our ... The individual will ensure that studies are conducted with appropriate quality, GLP compliance ...
$58.3K is the 25th percentile. Wages below this are outliers.
$44.4K - $61.2K
30% of jobs
$61.2K - $78.1K
9% of jobs
The median wage is $91K / yr.
$78.1K - $94.9K
14% of jobs
$94.9K - $111.7K
0% of jobs
$111.7K - $128.5K
0% of jobs
$128.5K - $145.3K
1% of jobs
$145.3K - $162.2K
3% of jobs
$177.2K is the 75th percentile. Wages above this are outliers.
$162.2K - $179K
20% of jobs
$179K - $195.8K
6% of jobs
$195.8K - $212.6K
9% of jobs
$212.6K - $229.5K
7% of jobs
$44.4K
$126.7K
$229.5K
| Aspect | Study Director | Laboratory Manager |
|---|---|---|
| Credentials | Typically requires advanced degrees (e.g., MS, PhD) and relevant certifications | Requires relevant degrees and management experience, but not necessarily advanced research credentials |
| Work Environment | Leads specific research or regulatory studies, often in contract labs or pharmaceutical companies | Oversees daily lab operations, staff, and compliance across multiple projects |
| Industry Usage | Commonly used in GLP, clinical, and research settings | Used broadly in laboratory settings across industries |
The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.
As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

Join Our Team as a Study Director and Research Scientist!
Your New Opportunity: We're all about teamwork. Every role contributes to the discovery, development, and manufacturing of new drug therapies, helping us get them to the people who need them faster. By living our values—Employee Development, Customer Focus, Quality and Excellence, Respect, and Integrity—we create a passionate, collaborative work environment. Whether you’re a recent graduate or seeking your next career move, your future could be with us.
Why Join Us?
The Role: Study Director, Research Scientist Are you passionate about preclinical research? As a Study Director, you’ll be the single point of control for assigned studies, responsible for the interpretation, analysis, documentation, and reporting of study results for both GLP and non-GLP studies.
What You’ll Do:
What You Need to Succeed:
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11 - 50 Employees
Fort Mill, SC, US
2018