Study Director I or II
Nelson, NE · On-site
The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study ...
Nelson, NE · On-site
The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study ...
Nelson, NE · On-site
The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study ...
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 ...
Boulder, CO · On-site
Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies
Boulder, CO · On-site
Works with study sponsors to create study protocols * Informs Live Phase Study Coordinator of decisions to initiate studies and thereby proceed with ordering animals and necessary study supplies
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
Oakland, NE · On-site
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
Oakland, NE · On-site
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide administrative and professional support for ...
New
About The Role Works under the guidance of designated Study Director(s), Contributing Scientists and Principal Investigators, as appropriate, to provide administrative and professional support for ...
New
Assists Study Directors on select projects under the direction and review of the Study Director team. Assists in collection, documentation and analysis of pre-clinical data. Assists in the ...
Assists Study Directors on select projects under the direction and review of the Study Director team. Assists in collection, documentation and analysis of pre-clinical data. Assists in the ...
Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...
Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
Job Summary The Consulting Study Director - Extractables & Leachables is a trusted advisor and consultative expert for clients and serves as the initial customer contact for extractable and leachable ...
Job Summary The Consulting Study Director - Extractables & Leachables is a trusted advisor and consultative expert for clients and serves as the initial customer contact for extractable and leachable ...
Oakland, NE · On-site
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
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Oakland, NE · On-site
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location. Key Responsibilities * Approve and sign study protocol * Ensure objectives meet regulatory requirements
Northwood, OH · On-site
Embrace collaboration, diverse perspectives and ideas. • Knows and understands the Animal Welfare Requirements and serves as a support to the Study Directors and/Principal Investigator, when ...
Northwood, OH · On-site
Embrace collaboration, diverse perspectives and ideas. • Knows and understands the Animal Welfare Requirements and serves as a support to the Study Directors and/Principal Investigator, when ...
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
Direct and/or supervise the work of technical staff in accordance with the GLP's * Monitor the progress of studies and after consultation with senior staff, report the results to the sponsor
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
As a Global Study Director (GSD), you will play a pivotal role in the Cell Therapy Clinical Operations organization, driving the operational planning and delivery of high-priority and complex ...
Austin, TX · On-site
$31 - $53/hr
Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...
Austin, TX · On-site
$31 - $53/hr
Support the Study Director in developing study protocols, amendments, and related documentation. * Facilitate cross-functional communication, establish and track study timelines, and prepare/lead ...
Jersey City, NJ · On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility) performed by the CSO. The CSD will ...
Jersey City, NJ · On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility) performed by the CSO. The CSD will ...
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility, ...) performed by the CSO. The CSD ...
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical activities (clinical part of CTD for registration, feasibility, ...) performed by the CSO. The CSD ...
$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
| 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.

The name Sotera Health was inspired by Soteria, the Greek goddess of safety, and reflects the Company's unwavering commitment to its mission, Safeguarding Global Health.
Sotera Health Company is a leading global provider of mission-critical sterilization and lab testing and advisory services for the healthcare industry. With a combined tenure across our businesses of nearly 200 years and our industry recognized scientific and technological expertise, we help to ensure the safety of millions of patients and healthcare practitioners around the world every year.
Across our 64 facilities worldwide, we have over 3,000 employees who are dedicated to safety and quality. We are a trusted partner to more than 5,800 customers in over 50 countries, including more than 40 of the top 50 medical device companies and 9 of the top 10 pharmaceutical companies.
Job Summary:
The Study Director has overall responsibility for the technical conduct of all assigned tests as well as for the review, interpretation, analysis, documentation, and reporting of results. The study director is the single point of study control. The study director ensures all assigned studies are completed on time.
Essential Duties:
Scientific/General
Regulatory Compliance
Customer Service
Project Management
Professionalism
Competencies of this position
Technical
Values
Professional
Work Environment:
This job operates in a professional laboratory environment. This role routinely uses standard office equipment and lab equipment including but not limited to computers keyboards, computer mouse, telephones, photocopiers, file cabinets, microscopes, micropipettes, pipette aids, various hand tools, and analytical equipment.
The possibility exists for exposure to biological and chemical hazards, exposure to carcinogenic compounds and other environmental aspects which may be considered unfavorable. Employees are expected to follow Biosafety and Chemical Hygiene policies, practices and procedures.
Travel:
Occasional local travel during the business day and occasional out of the area or overnight travel may be expected.
Physical requirements:
The physical demands described here are a representative of those that must be met to perform the essential job functions.
Education and experience requirements:
Sotera Health goes to market through its three best-in-class businesses - Sterigenics, Nordion and Nelson Labs. Sterigenics is a leading global provider of outsourced terminal sterilization and irradiation services for the medical device, pharmaceutical, food safety and advanced applications markets. Nordion is the leading global provider of Co-60 and gamma irradiators, which are key components to the gamma sterilization process. Nelson Labs is a global leader in outsourced microbiological and analytical chemistry testing and advisory services for the medical device and pharmaceutical industries.
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Health care and social assistance
1,001 - 5,000 Employees
Broadview Heights, OH, US
2017