The title, Study Director, refers to the individual responsible for the scientific conduct of assigned studies and should not be interpreted as department head, manager, director, etc. While this is ...
The title, Study Director, refers to the individual responsible for the scientific conduct of assigned studies and should not be interpreted as department head, manager, director, etc. While this is ...
Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed. May need to participate in study specific procedures. Evaluates ...
Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed. May need to participate in study specific procedures. Evaluates ...
Associate Study Director
Minneapolis, MN · On-site
$56K/yr
ISO, GMP, GLP) and NAMSA SOPs. • Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable. • Serves as the Study Director for GLP and non-GLP ...
Associate Study Director
Minneapolis, MN · On-site
$56K/yr
ISO, GMP, GLP) and NAMSA SOPs. • Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable. • Serves as the Study Director for GLP and non-GLP ...
ISO, GMP, GLP) and NAMSA SOPs. • Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable. • Serves as the Study Director for GLP and non-GLP ...
ISO, GMP, GLP) and NAMSA SOPs. • Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable. • Serves as the Study Director for GLP and non-GLP ...
Position Information Position Number 998733 Functional Title Assistant Director, Study Abroad Position Type Staff Position Eclass EP - EHRA 12 mo leave earning University Information Located in North ...
Position Information Position Number 998733 Functional Title Assistant Director, Study Abroad Position Type Staff Position Eclass EP - EHRA 12 mo leave earning University Information Located in North ...
Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed. May need to participate in study specific procedures. Evaluates ...
Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed. May need to participate in study specific procedures. Evaluates ...
Study Director, Rare Disease Translational Center
$85.99K - $133.68K/yr
Ensure studies are conducted in accordance with relevant regulatory requirements. Implement quality control measures to maintain the integrity, accuracy, and reliability of study data, including ...
Study Director, Rare Disease Translational Center
$85.99K - $133.68K/yr
Ensure studies are conducted in accordance with relevant regulatory requirements. Implement quality control measures to maintain the integrity, accuracy, and reliability of study data, including ...
Assistant Director, Study Abroad
Greensboro, NC · On-site
$50K - $51.42K/yr
Posting Details Position Information Position Number 998733 Functional Title Assistant Director, Study Abroad Position Type Staff Position Eclass EP - EHRA 12 mo leave earning University Information ...
Assistant Director, Study Abroad
Greensboro, NC · On-site
$50K - $51.42K/yr
Posting Details Position Information Position Number 998733 Functional Title Assistant Director, Study Abroad Position Type Staff Position Eclass EP - EHRA 12 mo leave earning University Information ...
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85.99K - $133.68K/yr
Key Responsibilities & Essential Functions • Develop and finalize study protocols, including experimental design, methodology, and timelines, in collaboration with cross-functional teams and ...
Study Director, Rare Disease Translational Center
Bar Harbor, ME · On-site
$85.99K - $133.68K/yr
Key Responsibilities & Essential Functions • Develop and finalize study protocols, including experimental design, methodology, and timelines, in collaboration with cross-functional teams and ...
Director, Study Start-Up
$195K - $275K/yr
... study startup activities, partnering with Quality Assurance as needed. Skills and experience you'll bring: * 10+ years of experience in the biotech/pharmaceutical industry with direct experience in ...
Director, Study Start-Up
$195K - $275K/yr
... study startup activities, partnering with Quality Assurance as needed. Skills and experience you'll bring: * 10+ years of experience in the biotech/pharmaceutical industry with direct experience in ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
... study start-up activities, partnering with Quality Assurance as needed. Skills and experience you'll bring: * 10+ years of experience in the biotech/pharmaceutical industry with direct experience in ...
Director, Study Start-Up
Watertown, MA · On-site
$195K - $275K/yr
... study start-up activities, partnering with Quality Assurance as needed. Skills and experience you'll bring: * 10+ years of experience in the biotech/pharmaceutical industry with direct experience in ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
CO · Hybrid
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
CO · Hybrid
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
Serve as the Principal Investigator/Study Director/Bioanalytical Monitor for internal and external studies. Has overall responsibility for the technical conduct of the study, interpretation and ...
Quick apply
Serve as the Principal Investigator/Study Director/Bioanalytical Monitor for internal and external studies. Has overall responsibility for the technical conduct of the study, interpretation and ...
*REVISED* Director of Study Abroad Programs, UNLV Global Education [R0151278]
Las Vegas, NV · On-site
Director of Study Abroad Programs, UNLV Global Education [R0151278] ROLE of the POSITION Reporting to the Senior Executive Director of UNLV Global, the Director of Study Abroad Programs ("Director ...
*REVISED* Director of Study Abroad Programs, UNLV Global Education [R0151278]
Las Vegas, NV · On-site
Director of Study Abroad Programs, UNLV Global Education [R0151278] ROLE of the POSITION Reporting to the Senior Executive Director of UNLV Global, the Director of Study Abroad Programs ("Director ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace! This position will be an integral part of the ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace!This position will be an integral part of the ...
Job Summary We are seeking an office-based Director of Study Start-Up to support our growing Study Start-Up/Regulatory Submissions team at Medpace!This position will be an integral part of the ...
Study Coordinator I
Ashland, OH · On-site
$49K - $57K/yr
Provide comments and/or suggested changes to Study Director/PI. * Proficient in generating reports in one major area. * Other duties as assigned by departmental management. QUALIFICATIONS:
Study Coordinator I
Ashland, OH · On-site
$49K - $57K/yr
Provide comments and/or suggested changes to Study Director/PI. * Proficient in generating reports in one major area. * Other duties as assigned by departmental management. QUALIFICATIONS:
Study Director/Senior Research Scientist
$85.70K - $109.20K/yr
Title may be flexible (e.g., Study Director, Senior Research Scientist, Principal Investigator) depending on experience and scope. Key Responsibilities: * Serve as the lead scientific authority ...
Study Director/Senior Research Scientist
$85.70K - $109.20K/yr
Title may be flexible (e.g., Study Director, Senior Research Scientist, Principal Investigator) depending on experience and scope. Key Responsibilities: * Serve as the lead scientific authority ...
Study Coordinator I
$49K - $57K/yr
Provide comments and/or suggested changes to Study Director/PI. * Proficient in generating reports in one major area. * Other duties as assigned by departmental management. QUALIFICATIONS:
Study Coordinator I
$49K - $57K/yr
Provide comments and/or suggested changes to Study Director/PI. * Proficient in generating reports in one major area. * Other duties as assigned by departmental management. QUALIFICATIONS:
Study Director information
See salary details
$59.1K is the 25th percentile. Wages below this are outliers.
$45K - $62K
30% of jobs
$62K - $79.1K
9% of jobs
The median wage is $92.2K / yr.
$79.1K - $96.1K
14% of jobs
$96.1K - $113.2K
0% of jobs
$113.2K - $130.2K
0% of jobs
$130.2K - $147.3K
1% of jobs
$147.3K - $164.3K
3% of jobs
$179.6K is the 75th percentile. Wages above this are outliers.
$164.3K - $181.4K
20% of jobs
$181.4K - $198.4K
6% of jobs
$198.4K - $215.5K
9% of jobs
$215.5K - $232.5K
7% of jobs
$45K
$128.4K
$232.5K
How much do study director jobs pay per year?
What Is the Job of a Study Director?
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.
What are the key skills and qualifications needed to thrive as a Study Director, and why are they important?
How does a Study Director typically collaborate with cross-functional teams during a research project?
What is a Study Director?
What job makes $10,000 a month without a degree?
What is the difference between Study Director vs Laboratory Manager?
| 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.
Job description
Position Summary
A Study Director has the overall technical responsibility of a study and functions as the liaison between the laboratory staff and the Project Manager. Responsibilities include supervising and coordinating activities of client projects, identifying areas of improvement and developing new processes, leading and managing the execution of assigned studies.
Essential Functions
- Provide strategic and technical oversight on studies.
- Collaborates on continuous process improvement opportunities.
- To draft study plans and contribute to the preparation of reports for sponsors.
- Function as the Subject Matter Expert (SME) on studies, particularly on sponsor calls.
- For any regulated studies, assure that:
- The study protocol (plan), including any change, is approved and is followed.
- All experimental data including observations of unanticipated responses of the test system are accurately recorded and verified.
- Unforeseen circumstances that may affect the quality and integrity of the study are noted when they occur, and corrective action is taken and documented.
- Test systems are as specified in the study protocol (plan).
- Regulatory agency's (e.g. FDA, EMA, etc.) guidelines are followed where appropriate.
- All raw data, documentation, protocols, specimens and final reports are transferred to the archives during or at the close of the study.
- To adhere to MedPharm's Procedures.
- Contribute to the preparation and review of SOPs and Forms where applicable.
- Where applicable, promptly record all data according to Good Documentation Practices.
- Review literature in preparation for studies and to regularly update knowledge by reviewing appropriate literature.
- Supervisory Responsibilities - This position may be responsible for training, assisting or assigning tasks to others.
- Any other duties and/or tasks that may be assigned.
- The studies that a study director would be leading are pre-clinical in vitro studies conducted at the MedPharm Research & Innovations site.
- Most of the assigned studies would include but are not limited to the following:
- In Vitro Release Testing (IVRT)
- In Vitro Permeation Testing (IVPT)
- Research Biology (e.g. various biological models, IVPT on various tissue constructs, etc.)
- The majority of the assigned studies will be conducted under R&D with a small percentage conducted under a regulated setting (e.g. in vitro bioequivalence).
Education and Experience
- Bachelor's degree in relevant scientific field (e.g. Chemistry, Biology, etc.)
- 3-5 years of relevant experience
- Proficiency in technical writing
- Must be able to analyze data sets and interpret results
- Familiarity with JMP is a plus, but not required
- Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams, etc.) required.
- Up to 5%
The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is occasionally required to walk; sit; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Other Duties
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.
About Medpharm.net
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
11 - 50 Employees
Headquarters location
Alexandria, VA, US