Study Director I
Nelson, NE ยท On-site
... 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 ...
Nelson, NE ยท On-site
... 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 ...
Nelson, NE ยท On-site
... 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 ...
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
New
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
New
New Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
New Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
Quick apply
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Education At least 5 years of experience directing non-clinical in vivo studies at a CRO or Pharmaceutical Company with a BS -or- At least 2 years of relevant industry/ toxicology experience with an ...
Quick apply
Education At least 5 years of experience directing non-clinical in vivo studies at a CRO or Pharmaceutical Company with a BS -or- At least 2 years of relevant industry/ toxicology experience with an ...
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
New
South Brunswick, NJ ยท On-site
Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics ... Supervise study conduct. * Assist in protocol development, design and implementation.
New
... pharmaceutical companies.## **Turn Science Into Successful Customer Outcomes**Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
... pharmaceutical companies.## **Turn Science Into Successful Customer Outcomes**Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
... pharmaceutical companies. Turn Science Into Successful Customer Outcomes Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
... pharmaceutical companies. Turn Science Into Successful Customer Outcomes Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
Jersey City, NJ ยท On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical ... in the pharmaceutical industry. Preferred Qualifications: Knowledge in ICH, GCP and local ...
Jersey City, NJ ยท On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical ... in the pharmaceutical industry. Preferred Qualifications: Knowledge in ICH, GCP and local ...
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
Bridgewater, NJ ยท On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical ... in the pharmaceutical industry. Preferred Qualifications: Knowledge in ICH, GCP and local ...
Bridgewater, NJ ยท On-site
The Clinical Study Director (CSD) is the medical reference in the clinical study and other clinical ... in the pharmaceutical industry. Preferred Qualifications: Knowledge in ICH, GCP and local ...
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
New
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
New
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
New
Demonstrated experience functioning as a Study Director within a CRO, pharmaceutical, biotechnology, or regulated research environment. * Experience leading GLP and non-GLP in vivo toxicology studies.
New
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
... pharmaceutical companies.## **Turn Science Into Successful Customer Outcomes**Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
... pharmaceutical companies.## **Turn Science Into Successful Customer Outcomes**Are you a science ... Study Directors serve as the key connection between our customers and laboratory teams, helping ...
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
Leads and directs teams in key study planning, development, and execution elements (e.g ... Bachelor's Degree and 9+ years of pharmaceutical, clinical drug development, project management ...
New
$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
For Pharmaceutical Study Director jobs, the most frequently searched job titles are:

Nelson, NE โข On-site
Full-time
Re-posted 4 days ago
Ensure the technical conduct of all assigned tests and review, interpret, analyze, document, and report results.
Maintain sample and data traceability, ensure raw data accuracy, and ensure test reports are compliant with procedures.
Coordinate workflow to meet sponsor expectations and ensure all studies are completed on time.
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:
Successful completion of Study Director Training.
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