Manage clinical trial operations from startup through closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with ICH-GCP and regulatory requirements
Quick apply
Manage clinical trial operations from startup through closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with ICH-GCP and regulatory requirements
Quick apply
Manage clinical trial operations from startup through closeout * Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with ICH-GCP and regulatory requirements
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 ...
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 ...
Richmond, VA ยท On-site
$80 - $100/hr
Responsibilities include participant recruitment, managing clinical trial operations, and contributing to data collection and analysis. Ideal candidates will be board certified in Family Medicine and ...
Richmond, VA ยท On-site
$80 - $100/hr
Responsibilities include participant recruitment, managing clinical trial operations, and contributing to data collection and analysis. Ideal candidates will be board certified in Family Medicine and ...
Oversee clinical trial operations, budgets, compliance, and workforce development * Chair the Research Operations Committee * Partner with Service Line Presidents to expand research programs
Oversee clinical trial operations, budgets, compliance, and workforce development * Chair the Research Operations Committee * Partner with Service Line Presidents to expand research programs
Fairfax, VA ยท On-site
$371K - $603K/yr
Oversee clinical trial operations, budgets, compliance, and workforce development * Chair the Research Operations Committee * Partner with Service Line Presidents to expand research programs
Fairfax, VA ยท On-site
$371K - $603K/yr
Oversee clinical trial operations, budgets, compliance, and workforce development * Chair the Research Operations Committee * Partner with Service Line Presidents to expand research programs
Norfolk, VA ยท On-site
$345K - $390K/yr
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Norfolk, VA ยท On-site
$345K - $390K/yr
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Norfolk, VA ยท On-site
$342K - $387K/yr
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Norfolk, VA ยท On-site
$342K - $387K/yr
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Expansion of system-wide clinical trial operations Benefits: * Flexible RVU structure to ensure adequate administrative and research time * Highly competitive salary * Academic appointments through ...
Educate potential and enrolled participants about the clinical trial, including procedures ... Collaborate with research staff to support smooth study operations in a fast-paced environment.
Quick apply
Educate potential and enrolled participants about the clinical trial, including procedures ... Collaborate with research staff to support smooth study operations in a fast-paced environment.
Triangle, VA ยท On-site
$100K - $140K/yr
Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms ... Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility ...
Triangle, VA ยท On-site
$100K - $140K/yr
Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms ... Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility ...
Triangle, VA ยท On-site
$100K - $140K/yr
Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms ... Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility ...
Triangle, VA ยท On-site
$100K - $140K/yr
Operational Planning: Develop study protocols, Informed Consent Forms (ICFs), Case Report Forms ... Oversee CROs, central labs, and clinical trial sites. Conduct site identification, feasibility ...
Fairfax, VA ยท On-site
$150 - $200/hr
Lead and execute Decentralized Clinical Trial (DCT) data auditing, oversight, and end-to-end study ... Oversee and coordinate daily clinical research operations, including regulatory submissions ...
Fairfax, VA ยท On-site
$150 - $200/hr
Lead and execute Decentralized Clinical Trial (DCT) data auditing, oversight, and end-to-end study ... Oversee and coordinate daily clinical research operations, including regulatory submissions ...
Fairfax, VA ยท On-site +1
$170K - $200K/yr
Lead and execute Decentralized Clinical Trial (DCT) data auditing, oversight, and end-to-end study ... Oversee and coordinate daily clinical research operations, including regulatory submissions ...
Fairfax, VA ยท On-site +1
$170K - $200K/yr
Lead and execute Decentralized Clinical Trial (DCT) data auditing, oversight, and end-to-end study ... Oversee and coordinate daily clinical research operations, including regulatory submissions ...
Newport News, VA ยท On-site
$502K - $650K/yr
Mentor practitioners in clinical trial development and encourage physician, APP, pharmacist, and ... operational oversight. The alliance will establish a Joint Clinical Trials Program Steering ...
Newport News, VA ยท On-site
$502K - $650K/yr
Mentor practitioners in clinical trial development and encourage physician, APP, pharmacist, and ... operational oversight. The alliance will establish a Joint Clinical Trials Program Steering ...
$502K - $650K/yr
Mentor practitioners in clinical trial development and encourage physician, APP, pharmacist, and ... operational oversight. The alliance will establish a Joint Clinical Trials Program Steering ...
$502K - $650K/yr
Mentor practitioners in clinical trial development and encourage physician, APP, pharmacist, and ... operational oversight. The alliance will establish a Joint Clinical Trials Program Steering ...
Reviewing the performance dashboards and other clinical trial systems to oversee site and patient ... operational aspects (required visits/calls, duration, and frequency); * Ensuring adherence to ...
Reviewing the performance dashboards and other clinical trial systems to oversee site and patient ... operational aspects (required visits/calls, duration, and frequency); * Ensuring adherence to ...
Richmond, VA ยท On-site
$160K - $240K/yr
... trial recruitment and retention; collaborate with clinical operations toidentifyandfacilitateresolution of investigator site issues. Essential Requirements * Advanced degree in a scientific ...
Richmond, VA ยท On-site
$160K - $240K/yr
... trial recruitment and retention; collaborate with clinical operations toidentifyandfacilitateresolution of investigator site issues. Essential Requirements * Advanced degree in a scientific ...
Charlottesville, VA ยท On-site
$50 - $55/hr
The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development ... Participate in activities that will further the operational development of Science 37 nursing ...
Charlottesville, VA ยท On-site
$50 - $55/hr
The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development ... Participate in activities that will further the operational development of Science 37 nursing ...
Charlottesville, VA ยท On-site
$50 - $55/hr
The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development ... Participate in activities that will further the operational development of Science 37 nursing ...
Charlottesville, VA ยท On-site
$50 - $55/hr
The Nursing Solutions Group is involved throughout the trial life cycle, from protocol development ... Participate in activities that will further the operational development of Science 37 nursing ...
$17.16 - $21.93
4% of jobs
$21.93 - $26.69
8% of jobs
$26.69 - $31.46
12% of jobs
$31.60 is the 25th percentile. Wages below this are outliers.
$31.46 - $36.22
26% of jobs
$36.22 - $40.99
18% of jobs
$42.65 is the 75th percentile. Wages above this are outliers.
$40.99 - $45.76
19% of jobs
$45.76 - $50.52
6% of jobs
$50.52 - $55.29
2% of jobs
$55.29 - $60.06
1% of jobs
$60.06 - $64.82
1% of jobs
$64.82 - $69.59
2% of jobs
$17
$39
$69
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.
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.
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.
The most popular types of Clinical Trial Operations jobs in Virginia are:
For Clinical Trial Operations jobs in Virginia, the most frequently searched job titles are:
The top searched job categories for Clinical Trial Operations jobs in Virginia are:

Full-time
Re-posted 27 days ago
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.
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
Sourced by ZipRecruiter
51 - 200 Employees
Chantilly, VA, US
2004