Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Quick apply
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices. Requirements Key Responsibilities ...
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices. Requirements Key Responsibilities ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Quick apply
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Manage clinical trial operations from startup to closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB ...
Operations Manager Clinical Trials
$41 - $56/hr
Temporary Contract (15 Weeks) Schedule: Monday - Friday | 8:30 AM - 5:00 PM Pay: $41.00 - $56.00 ... The ideal candidate has strong leadership skills, experience managing clinical trial operations ...
Quick apply
Operations Manager Clinical Trials
$41 - $56/hr
Temporary Contract (15 Weeks) Schedule: Monday - Friday | 8:30 AM - 5:00 PM Pay: $41.00 - $56.00 ... The ideal candidate has strong leadership skills, experience managing clinical trial operations ...
... clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure). Additional Information Regards Rahul ...
... clinical research experience, including 4 years of strong trial operations management experience across all study periods (start-up, maintenance and closure). Additional Information Regards Rahul ...
Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and ...
Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and ...
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for the strategic planning and analytics capability to support current and future Legend pipeline studies.
Role Overview The Sr. Manager, Clinical Trial Operations Planning & Analytics is responsible for the strategic planning and analytics capability to support current and future Legend pipeline studies.
Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and ...
Summary The Associate Director for Clinical Trial Operations and Workforce Development provides strategic and operational leadership for clinical trial activities within the Clinical and ...
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset , NJ . Role Overview The Sr. Manager, Clinical Trial ...
Legend Biotech is seeking a Sr. Manager, Clinical Trial Operations Planning & Analytics as part of the Clinical Operations team based in Somerset , NJ . Role Overview The Sr. Manager, Clinical Trial ...
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · Remote
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Quick apply
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
Clinical Trial Manager
San Diego, CA · On-site
$110K - $140K/yr
Manages trial operational plan and CRO activities, including project timelines & quality of deliverables, and managing approved trial budget(s) throughout the life of the assigned clinical trial(s)
The candidate will act as the Clinical Trial Manager in the implementation of Investigator Sponsored Trials primarily in Diabetes, but may include other therapeutic areas. Key responsibilities will ...
The candidate will act as the Clinical Trial Manager in the implementation of Investigator Sponsored Trials primarily in Diabetes, but may include other therapeutic areas. Key responsibilities will ...
Direct end-to-end clinical trial operations activities domestically and globally: i.e. lead and take ownership in all aspects of Study Operations for CAR-T Studies in a matrix environment.
Direct end-to-end clinical trial operations activities domestically and globally: i.e. lead and take ownership in all aspects of Study Operations for CAR-T Studies in a matrix environment.
Clinical Trial Planning and Analytics (CTP&A) is accountable for endtoend clinical trial ... The Clinical Trial Operations Technology function is responsible for the strategic ownership ...
Clinical Trial Planning and Analytics (CTP&A) is accountable for endtoend clinical trial ... The Clinical Trial Operations Technology function is responsible for the strategic ownership ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
The Trial Supplies Operations Manager is responsible for the implementation of appropriate Clinical Supplies strategies and processes in order to achieve clinical study objectives in assigned ...
Clinical Trial Manager
Blue Bell, PA · On-site
Local Operations Manager - Advanced - Immunology ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
Clinical Trial Manager
Blue Bell, PA · On-site
Local Operations Manager - Advanced - Immunology ICON is a global healthcare intelligence and ... As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities ...
Temporary Clinical Trial Operations information
See salary details
$17.31 - $22.12
4% of jobs
$22.12 - $26.92
8% of jobs
$26.92 - $31.73
12% of jobs
$31.88 is the 25th percentile. Wages below this are outliers.
$31.73 - $36.54
26% of jobs
$36.54 - $41.35
18% of jobs
$43.02 is the 75th percentile. Wages above this are outliers.
$41.35 - $46.15
19% of jobs
$46.15 - $50.96
6% of jobs
$50.96 - $55.77
2% of jobs
$55.77 - $60.58
1% of jobs
$60.58 - $65.38
1% of jobs
$65.38 - $70.19
2% of jobs
$17
$39
$70
How much do temporary clinical trial operations jobs pay per hour?
As of Jun 17, 2026, the average hourly pay for temporary clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.
What is the difference between Temporary Clinical Trial Operations vs Clinical Trial Coordinators?
| Aspect | Temporary Clinical Trial Operations | Clinical Trial Coordinators |
|---|---|---|
| Credentials | Relevant experience, sometimes certifications in clinical research | Often require a degree in health sciences or related field, plus certification |
| Work Environment | Contract-based, project-specific settings within research organizations | Typically office-based, coordinating daily trial activities |
| Employer & Industry Usage | Used by CROs, pharmaceutical companies for short-term needs | Commonly employed by research sites and hospitals |
Temporary Clinical Trial Operations roles focus on short-term, project-specific tasks within clinical research, often requiring specialized experience or certifications. Clinical Trial Coordinators handle ongoing trial management and participant coordination, usually with a background in health sciences. Both roles are essential in the clinical research process but differ mainly in duration, scope, and employment setting.
More about Temporary Clinical Trial Operations jobs
What cities are hiring for Temporary Clinical Trial Operations jobs? Cities with the most Temporary Clinical Trial Operations job openings:
What are the most commonly searched types of Clinical Trial Operations jobs? The most popular types of Clinical Trial Operations jobs are:
What states have the most Temporary Clinical Trial Operations jobs? States with the most job openings for Temporary Clinical Trial Operations jobs include:
What job categories do people searching Temporary Clinical Trial Operations jobs look for? The top searched job categories for Temporary Clinical Trial Operations jobs are:
- Contract Clinical Trial Data Transparency
- Remote Clinical Research Phlebotomist
- Clinical Trials
- Associate Clinical Trial Manager
- Clinical Trial Research Coordinator
- Clinical Research Associate
- Remote Clinical Trials
- Entry Level Clinical Study Startup
- History Research Assistant
- Remote Pfizer Clinical Research
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Posted 4 days ago
Job description
Description
Clinical Trial & Pharmacovigilance Manager
Location: Hybrid
Job Type: Full-Time
Position Overview:
Venesco is seeking an experienced Clinical Trial & Pharmacovigilance Manager to oversee clinical trial operations and ensure robust safety surveillance practices.
Requirements
Key Responsibilities: Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB activities and safety reviews Develop and maintain clinical study documentation Collaborate with regulatory teams on submissions
Minimum Qualifications: Advanced degree in clinical research, life sciences, or related healthcare field 8+ years of clinical operations and safety experience Strong knowledge of ICH-GCP and FDA regulations
Preferred Qualifications: Experience with Argus or ArisG safety databases Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
About Venesco
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Chantilly, VA, US
Year founded
2004