Direct Phase I and Phase II clinical trial operations. * Lead pharmacovigilance and safety surveillance activities. * Develop and maintain product safety profiles. * Oversee adverse event collection ...
Direct Phase I and Phase II clinical trial operations. * Lead pharmacovigilance and safety surveillance activities. * Develop and maintain product safety profiles. * Oversee adverse event collection ...
Direct Phase I and Phase II clinical trial operations. * Lead pharmacovigilance and safety surveillance activities. * Develop and maintain product safety profiles. * Oversee adverse event collection ...
Quick apply
Direct Phase I and Phase II clinical trial operations. * Lead pharmacovigilance and safety surveillance activities. * Develop and maintain product safety profiles. * Oversee adverse event collection ...
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 ...
Associate Director, Clinical Trial Management
$34.25 - $46.75/hr
Coordinates clinical trial operational activities to ensure completion according to project timelines and budget * Ensure clinical trials are conducted in compliance with NewAmsterdam Pharma SOPs ...
Associate Director, Clinical Trial Management
$34.25 - $46.75/hr
Coordinates clinical trial operational activities to ensure completion according to project timelines and budget * Ensure clinical trials are conducted in compliance with NewAmsterdam Pharma SOPs ...
Operations Manager Clinical Trials
Miami, FL · On-site
$41 - $56/hr
The ideal candidate has strong leadership skills, experience managing clinical trial operations, and a thorough understanding of FDA regulations, Good Clinical Practice (GCP), and clinical research ...
Quick apply
Operations Manager Clinical Trials
Miami, FL · On-site
$41 - $56/hr
The ideal candidate has strong leadership skills, experience managing clinical trial operations, and a thorough understanding of FDA regulations, Good Clinical Practice (GCP), and clinical research ...
Provide day-to-day accountability for the operational delivery of assigned clinical trials ... Ensure all trial records meet quality and compliance standards. What You'll Need: * Bachelor ...
Provide day-to-day accountability for the operational delivery of assigned clinical trials ... Ensure all trial records meet quality and compliance standards. What You'll Need: * Bachelor ...
Position Overview The Senior Director, Clinical Field Monitoring and Trial Operations (FMTO) provides strategic and operational leadership for Immunome's clinical trial monitoring function ...
New
Position Overview The Senior Director, Clinical Field Monitoring and Trial Operations (FMTO) provides strategic and operational leadership for Immunome's clinical trial monitoring function ...
New
Position Overview The Senior Director, Clinical Field Monitoring and Trial Operations (FMTO) provides strategic and operational leadership for Immunome's clinical trial monitoring function ...
Position Overview The Senior Director, Clinical Field Monitoring and Trial Operations (FMTO) provides strategic and operational leadership for Immunome's clinical trial monitoring function ...
As the Clinical Trial Manager of Clinical Operations, initially reporting to the Director, Clinical Operations, you will be responsible for Contract Research Organization (CRO) oversight and ...
As the Clinical Trial Manager of Clinical Operations, initially reporting to the Director, Clinical Operations, you will be responsible for Contract Research Organization (CRO) oversight and ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements. * Participate in reviewing, formatting, and finalizing study-related ...
Quick apply
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements. * Participate in reviewing, formatting, and finalizing study-related ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements. * Participate in reviewing, formatting, and finalizing study-related ...
Clinical Trial Associate
Needham, MA · On-site
$88K - $100K/yr
Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements. * Participate in reviewing, formatting, and finalizing study-related ...
Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
As a key contributor within Clinical Operations, you'll help drive the development of our first clinical stage autologous cell therapy trial targeting solid tumors. You'll play a key role in driving ...
Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
As a key contributor within Clinical Operations, you'll help drive the development of our first clinical stage autologous cell therapy trial targeting solid tumors. You'll play a key role in driving ...
Clinical Trial Manager
Princeton, NJ · On-site
As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...
Clinical Trial Manager
Princeton, NJ · On-site
As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...
Senior Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
As a key contributor within Clinical Operations, you'll help to drive the development of our first clinical stage autologous cell therapy trial targeting solid tumors. You'll play a key role in ...
Senior Clinical Trial Associate - Oncology
Bedford, MA · Hybrid
$35.25 - $48/hr
As a key contributor within Clinical Operations, you'll help to drive the development of our first clinical stage autologous cell therapy trial targeting solid tumors. You'll play a key role in ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Clinical Trial Manager is an experienced clinical operations professional responsible for ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Clinical Trial Manager is an experienced clinical operations professional responsible for ...
Clinical Trial Associate
$36.50 - $49.75/hr
Support clinical trial operations across all phases of the study lifecycle, ensuring milestones, deliverables, timelines, and budgets are met. * Assist with CRO and vendor coordination and oversight ...
Clinical Trial Associate
$36.50 - $49.75/hr
Support clinical trial operations across all phases of the study lifecycle, ensuring milestones, deliverables, timelines, and budgets are met. * Assist with CRO and vendor coordination and oversight ...
Clinical Trial Manager II
Boston, MA · On-site
$120K - $180K/yr
The Clinical Trial Manager II (CTM II) is responsible for the delivery of all clinical aspects of ... Participate in program strategy meetings, ad hoc clinical operations' initiatives and programs ...
Clinical Trial Manager II
Boston, MA · On-site
$120K - $180K/yr
The Clinical Trial Manager II (CTM II) is responsible for the delivery of all clinical aspects of ... Participate in program strategy meetings, ad hoc clinical operations' initiatives and programs ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Clinical Trial Manager is an experienced clinical operations professional responsible for ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Clinical Trial Manager is an experienced clinical operations professional responsible for ...
Clinical Sample Manager
Sioux Falls, SD · On-site +1
$130K - $150K/yr
Provide operational oversight of assigned clinical trial service providers, ensuring services are delivered according to study requirements, quality standards, and timelines. * Serve as the primary ...
Clinical Sample Manager
Sioux Falls, SD · On-site +1
$130K - $150K/yr
Provide operational oversight of assigned clinical trial service providers, ensuring services are delivered according to study requirements, quality standards, and timelines. * Serve as the primary ...
Director, Clinical Trial Quality & Risk Management, National Center for Clinical Trials (NCCT)
$63.45 - $95.20/hr
Facilitate operational ownership and escalation of corrective and preventative actions (CAPAs ... Partner with Clinical Trial Operations and enterprise stakeholders to reinforce training and ...
Director, Clinical Trial Quality & Risk Management, National Center for Clinical Trials (NCCT)
$63.45 - $95.20/hr
Facilitate operational ownership and escalation of corrective and preventative actions (CAPAs ... Partner with Clinical Trial Operations and enterprise stakeholders to reinforce training and ...
Commission 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 commission clinical trial operations jobs pay per hour?

Full-time
Re-posted 28 days ago
Job description
Description
Clinical Trial & Pharmacovigilance Manager
Venesco LLC is seeking a Clinical Trial & Pharmacovigilance Manager to lead clinical operations and drug safety surveillance activities across multiple FDA-regulated clinical development programs. This individual will provide strategic oversight for clinical trial execution, adverse event management, safety surveillance, and regulatory compliance while leading multidisciplinary teams.
Requirements
Duties and Responsibilities
- Direct Phase I and Phase II clinical trial operations.
- Lead pharmacovigilance and safety surveillance activities.
- Develop and maintain product safety profiles.
- Oversee adverse event collection, coding, review, and reporting.
- Manage DSMB activities and implementation of recommendations.
- Ensure compliance with FDA, ICH, and sponsor requirements.
- Coordinate safety reviews, risk assessments, and signal detection activities.
- Lead development of safety management plans and surveillance plans.
- Manage cross-functional teams including monitors, safety personnel, and clinical operations staff.
- Support INDs, Investigator Brochures, DSURs, annual reports, and safety submissions.
- Develop SOPs and improve operational processes.
Minimum Qualifications
- Advanced degree in Clinical Research, Nursing, Pharmacy, Public Health, or Life Sciences.
- Minimum 10 years of clinical research experience.
- Demonstrated leadership of Phase I and Phase II clinical studies.
- Strong expertise in ICH-GCP and FDA clinical research requirements.
- Experience managing clinical operations and pharmacovigilance programs.
- Proven ability to lead multidisciplinary teams.
Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.
For more information on Venesco, LLC., visit https://venesco.com.
About Venesco
Sourced by ZipRecruiter
Company size
51 - 200 Employees
Headquarters location
Chantilly, VA, US
Year founded
2004