Develop and maintain clinical study documentation * Collaborate with regulatory teams on ... Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
Quick apply
Develop and maintain clinical study documentation * Collaborate with regulatory teams on ... Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
Quick apply
Develop and maintain clinical study documentation * Collaborate with regulatory teams on ... Clinical trial management certification MUST BE A US CITIZEN and US Board certified MD
Description Clinical Trial & Pharmacovigilance Manager Location: Hybrid Job Type: Full-Time ... clinical study documentation Collaborate with regulatory teams on submissions Minimum ...
Description Clinical Trial & Pharmacovigilance Manager Location: Hybrid Job Type: Full-Time ... clinical study documentation Collaborate with regulatory teams on submissions Minimum ...
... clinical study documentation โข Collaborate with regulatory teams on submissions Minimum ... management certification MUST BE A US CITIZEN and US Board certified MD
... clinical study documentation โข Collaborate with regulatory teams on submissions Minimum ... management certification MUST BE A US CITIZEN and US Board certified MD
This role combines strategic oversight with hands-on study coordination, supporting protocol ... Hands-on experience with REDCap for clinical research data capture and management * Ability to work ...
Quick apply
This role combines strategic oversight with hands-on study coordination, supporting protocol ... Hands-on experience with REDCap for clinical research data capture and management * Ability to work ...
Fairfax, VA ยท On-site +1
$170K - $200K/yr
This role combines strategic oversight with hands-on study coordination, supporting protocol ... Hands-on experience with REDCap for clinical research data capture and management * Ability to work ...
Fairfax, VA ยท On-site +1
$170K - $200K/yr
This role combines strategic oversight with hands-on study coordination, supporting protocol ... Hands-on experience with REDCap for clinical research data capture and management * Ability to work ...
Bethesda, MD ยท On-site
Clinical Biostatistician Responsibilities Include: Statistical Programming & Validation * Develop ... study teams. * Ability to work independently, manage shifting priorities, and deliver high-quality ...
Bethesda, MD ยท On-site
Clinical Biostatistician Responsibilities Include: Statistical Programming & Validation * Develop ... study teams. * Ability to work independently, manage shifting priorities, and deliver high-quality ...
Washington, DC ยท On-site +1
... and managed, and support the communities we serve. This is hard, urgent, selfless work-but it ... Plan clinical study data analysis and lead interpretation of clinical study results. * Support ...
Washington, DC ยท On-site +1
... and managed, and support the communities we serve. This is hard, urgent, selfless work-but it ... Plan clinical study data analysis and lead interpretation of clinical study results. * Support ...
$17.20 - $30.30/hr
Participate in clinical study start-up meetings. Assist research nurses, study coordinators ... Management and Analysis - Awareness Interpersonal Skills - Awareness Oral and Written ...
$17.20 - $30.30/hr
Participate in clinical study start-up meetings. Assist research nurses, study coordinators ... Management and Analysis - Awareness Interpersonal Skills - Awareness Oral and Written ...
This will include the creation of overall clinical development plans and clinical study design ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
This will include the creation of overall clinical development plans and clinical study design ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Washington, DC ยท On-site
$17.20 - $30.30/hr
Participate in clinical study start-up meetings. * Assist research nurses, study coordinators ... Clinical Trial Management System - Awareness * Data Entry - Awareness * Data Collection and ...
Washington, DC ยท On-site
$17.20 - $30.30/hr
Participate in clinical study start-up meetings. * Assist research nurses, study coordinators ... Clinical Trial Management System - Awareness * Data Entry - Awareness * Data Collection and ...
Rockville, MD ยท On-site +1
... study sites either onsite at investigative sites or remotely to ensure clinical trials are ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...
Rockville, MD ยท On-site +1
... study sites either onsite at investigative sites or remotely to ensure clinical trials are ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...
Bethesda, MD ยท On-site
$82K - $109K/yr
This role involves translating clinical study requirements into technical specifications and ... Clinical Data Management: Creates and maintains study data management documents according to ...
Bethesda, MD ยท On-site
$82K - $109K/yr
This role involves translating clinical study requirements into technical specifications and ... Clinical Data Management: Creates and maintains study data management documents according to ...
This role involves translating clinical study requirements into technical specifications and ... Clinical Data Management: Creates and maintains study data management documents according to ...
This role involves translating clinical study requirements into technical specifications and ... Clinical Data Management: Creates and maintains study data management documents according to ...
Oversight of clinical operations activities, including one or more of the following: clinical project management, clinical site management (essential regulatory documents, study start up, site ...
Oversight of clinical operations activities, including one or more of the following: clinical project management, clinical site management (essential regulatory documents, study start up, site ...
Rockville, MD ยท On-site
... study sites either onsite at investigative sites or remotely to ensure clinical trials are ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...
Rockville, MD ยท On-site
... study sites either onsite at investigative sites or remotely to ensure clinical trials are ... CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring ...
Rockville, MD ยท On-site
Contribute to developing study protocols, statistical analysis plans, and clinical study reports. * Collaborate with Database Development on study database, eCRF, and edit checks design. * Manage ...
Rockville, MD ยท On-site
Contribute to developing study protocols, statistical analysis plans, and clinical study reports. * Collaborate with Database Development on study database, eCRF, and edit checks design. * Manage ...
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Washington, DC ยท On-site +1
Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and closeout activities (onsite, virtual, remote)
Washington, DC ยท On-site +1
Study & Site Management * Serve as CRA for assigned complex clinical studies, providing expert oversight of site selection, initiation, monitoring, and closeout activities (onsite, virtual, remote)
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
Gaithersburg, MD ยท On-site
$249K - $374K/yr
This will include the creation of overall clinical development plans and clinical study design as ... Demonstrated experience managing complex projects and working collaboratively with multiple ...
$32.67 - $39.60
4% of jobs
$39.60 - $46.53
6% of jobs
$46.53 - $53.46
7% of jobs
$58.66 is the 25th percentile. Wages below this are outliers.
$53.46 - $60.39
9% of jobs
$60.39 - $67.32
15% of jobs
The median wage is $70.38 / hr.
$67.32 - $74.25
18% of jobs
$79.19 is the 75th percentile. Wages above this are outliers.
$74.25 - $81.18
21% of jobs
$81.18 - $88.11
7% of jobs
$88.11 - $95.04
6% of jobs
$95.04 - $101.97
3% of jobs
$101.97 - $108.90
2% of jobs
$32
$70
$108
The most popular types of Clinical Study jobs in Washington are:
For Clinical Study Manager jobs in Washington, the most frequently searched job titles are:
The top searched job categories for Clinical Study Manager jobs in Washington are:
Cities in Washington with the most Clinical Study Manager job openings:

Full-time
Re-posted 21 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