Triangle, VA · On-site
$100K - $140K/yr
Study Leadership: Lead the end-to-end management of multiple clinical studies, including ... Ability to work in a fast-paced, "startup" environment. #LI-NK1 $100,000 - $140,000 The expected ...
Triangle, VA · On-site
$100K - $140K/yr
Study Leadership: Lead the end-to-end management of multiple clinical studies, including ... Ability to work in a fast-paced, "startup" environment. #LI-NK1 $100,000 - $140,000 The expected ...
Study Leadership: Lead the end-to-end management of multiple clinical studies, including ... Ability to work in a fast-paced, "startup" environment. #LI-NK1 $100,000 - $140,000 The expected ...
Study Leadership: Lead the end-to-end management of multiple clinical studies, including ... Ability to work in a fast-paced, "startup" environment. #LI-NK1 $100,000 - $140,000 The expected ...
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Virginia Beach, VA · On-site
$120 - $180/hr
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Virginia Beach, VA · On-site
$120 - $180/hr
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Richmond, VA · On-site
$120 - $180/hr
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Richmond, VA · On-site
$120 - $180/hr
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Quick apply
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Quick apply
Oversee processes for referral intake, scheduling, patient navigation, study startup, and protocol feasibility. * Supervise implementation of CTMS, EHR, and other clinical documentation systems.
Manage clinical trial operations from startup through closeout * Oversee adverse event reporting ... Develop and maintain clinical study documentation * Collaborate with regulatory teams on ...
Quick apply
Manage clinical trial operations from startup through closeout * Oversee adverse event reporting ... Develop and maintain clinical study documentation * Collaborate with regulatory teams on ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and ... clinical study documentation Collaborate with regulatory teams on submissions Minimum ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and ... clinical study documentation Collaborate with regulatory teams on submissions Minimum ...
Requirements Key Responsibilities: • Manage clinical trial operations from startup through ... clinical study documentation • Collaborate with regulatory teams on submissions Minimum ...
Requirements Key Responsibilities: • Manage clinical trial operations from startup through ... clinical study documentation • Collaborate with regulatory teams on submissions Minimum ...
Virginia Beach, VA · On-site +1
... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...
Virginia Beach, VA · On-site +1
... clinical trials across all phases from study start-up to close-out. Responsabilities: * Provide oversight and expertise for imaging setup and startup activities * Maintain the quality and scientific ...
$71K - $145K/yr
... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
$71K - $145K/yr
... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
Fairfax, VA · On-site
$71K - $145K/yr
... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
Fairfax, VA · On-site
$71K - $145K/yr
... clinical research studies by performing site monitoring and site management activities. In this ... startup activities based on study needs. Accurate and timely documentation is critical. The CRA I ...
Charlottesville, VA · On-site
$108K - $147K/yr
Reconcile non-sponsored research study accounts, identifying revenue/expense variances and working ... Analyze clinical billing and revenue trends to support assessment of provider productivity and ...
New
Charlottesville, VA · On-site
$108K - $147K/yr
Reconcile non-sponsored research study accounts, identifying revenue/expense variances and working ... Analyze clinical billing and revenue trends to support assessment of provider productivity and ...
New
Roanoke, VA · On-site +1
$25.50 - $33.75/hr
After running a successful pilot study with results that exceeded all expectations, the team is ... Learn new clinical protocols quickly * Communicate well with both patients and providers * Have ...
Roanoke, VA · On-site +1
$25.50 - $33.75/hr
After running a successful pilot study with results that exceeded all expectations, the team is ... Learn new clinical protocols quickly * Communicate well with both patients and providers * Have ...
Hampton, VA · On-site
$203.16 - $263.84/hr
... studies in CSU, ColdU, SD and phase 2 studies in AD and PN. We're looking for curious, driven ... Proven ability to create training from scratch in a fast-paced, startup environment * Excellent ...
Hampton, VA · On-site
$203.16 - $263.84/hr
... studies in CSU, ColdU, SD and phase 2 studies in AD and PN. We're looking for curious, driven ... Proven ability to create training from scratch in a fast-paced, startup environment * Excellent ...
| Aspect | Freelance Clinical Study Startup | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires knowledge of clinical trial processes, basic certifications, or relevant experience | Requires a degree in life sciences or healthcare, and often certifications like CCRP or RAC |
| Work Environment | Independent, project-based, often remote or on-site at trial locations | Usually employed by sponsors or CROs, working on-site or remotely within a structured team |
| Employer & Industry Usage | Freelance roles in biotech, pharma, or CROs managing startup phases of trials | Full-time or contract roles within pharmaceutical companies or CROs overseeing trial conduct |
In summary, a Freelance Clinical Study Startup focuses on initiating and managing early trial phases independently, while a Clinical Research Associate typically works within a team to monitor ongoing trials, requiring more formal certifications and a structured work environment.
The most popular types of Clinical Study Startup jobs in Virginia are:
For Freelance Clinical Study Startup jobs in Virginia, the most frequently searched job titles are:
The top searched job categories for Freelance Clinical Study Startup jobs in Virginia are:
Cities in Virginia with the most Freelance Clinical Study Startup job openings:
Triangle, VA • On-site
$100K - $140K/yr
Full-time
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