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Clinical Trial Operations Jobs (NOW HIRING)

Candel Therapeutics

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 ...

Candel Therapeutics

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 ...

Kardigan

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 ...

Kura Oncology

Clinical Trial Associate

Boston, MA

$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 ...

SAB

Clinical Sample Manager

Sioux Falls, SD · Remote

$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 ...

SAB

Clinical Trial Manager, Immunology

Miami Beach, FL · Remote

$150K - $165K/yr

Manage all aspects of clinical trial operations, ensuring adherence to timelines, budgets, and regulatory requirements. * Participate in the identification, evaluation, selection, and oversight of ...

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Clinical Trial Operations information

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How much do clinical trial operations jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for 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 are the key skills and qualifications needed to thrive in clinical trial operations?

To thrive in Clinical Trial Operations, you typically need a background in life sciences or healthcare, strong project management abilities, and familiarity with clinical research protocols and regulatory guidelines. Experience with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are often required. Excellent organizational, communication, and problem-solving skills help you collaborate effectively with cross-functional teams and manage complex study logistics. These competencies are crucial to ensuring clinical trials run smoothly, efficiently, and in compliance with industry standards.

What is a clinical trial operations?

A Clinical Trial Operations job involves overseeing the planning, execution, and management of clinical trials to ensure they comply with regulatory guidelines and study protocols. Professionals in this role coordinate with investigators, sponsors, and regulatory agencies to ensure trials run smoothly and efficiently. They manage timelines, budgets, patient recruitment, data collection, and compliance with ethical and legal standards. Their ultimate goal is to ensure the trial produces reliable data while prioritizing patient safety.

What are the typical daily responsibilities in clinical trial operations?

A clinical trial operations professional oversees the planning, implementation, and management of clinical research studies. Daily tasks often include coordinating study timelines, monitoring site performance, ensuring adherence to regulatory requirements, managing study documentation, and communicating with trial sites and sponsors. The role also involves addressing operational issues quickly and adjusting plans as needed to keep the trial on track. This position usually works closely with principal investigators, data managers, regulatory teams, and sponsors, making collaboration and communication essential for success.

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Clinical Trial Operations jobs near you
Infographic showing various Clinical Trial Operations job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Trial & Pharmacovigilance Manager

VENESCO, LLC

Fort Detrick, MD • On-site

Full-time

Re-posted 27 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.

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