Top 40 Clinical trial manager Jobs in Fairfax Va

MedTech Site Manager 1
IQVIA —Washington, DC
- $74,500 - $124,100 a year
- Full-time
- Remote
- Bachelor of Science
- Mid-level
- Team management
- Work from home
3d
Associate Account Manager - Clinical Trial Division - West Coast, US
Thermo Fisher Scientific —Washington, DC
- $76,700 - $115,025 a year
- Online Application
- Hybrid work
- Research
- Mid-level
- Master's degree
- Commuter assistance
- Paid parental leave
12d
Brain Injury and Health Project Manager
Henry M. Jackson Foundation —Silver Spring, MD
- $73,800 - $125,600 a year
- Full-time
- Management
- Senior level
- Health insurance
- Dental insurance
Manager / Sr. Manager, Clinical Operations - FSP West Region
Thermo Fisher Scientific —Washington, DC
- $115,000 - $178,000 a year
- Full-time
- Remote
- English
- Business development
- Travel
- Commuter assistance
- Paid parental leave
11d
TBI Research Activities Manager
Henry M. Jackson Foundation —Silver Spring, MD
- $88,600 - $150,800 a year
- Full-time
- Senior level
- Health insurance
- Dental insurance
Clinical Trial & Pharmacovigilance Manager
VENESCO, LLC —Falls Church, VA
- Full-time
- Medicine
- Management
- Databases
Quick Apply
Manager, Clinical Research Operations
George Washington University —Foggy Bottom, DC
- $76,088.27 - $123,763.85 a year
- Full-time
- Background check
- Management
- Bachelor of Science
- Disability insurance
- Health insurance
6d
Sr. TMF Manager
MacroGenics, Inc. —Rockville, MD
- $144,300 - $220,000 a year
- Remote
- 7 years
- Computer Science
- Bachelor's degree
- Paid parental leave
- Employee stock purchase plan
Quick Apply
11d
Clinical Program Manager
GAP SOLUTIONS INC —Bethesda, MD
- $125,000 - $185,000 a year
- Email
- Nursing
- Writing skills
- Master's degree
Quick Apply
Senior Global Clinical Study Manager
IQVIA —Rockville, MD
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —Washington, DC
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Scientific Outreach/Partnerships Manager - NIH
Global Solutions Network Inc —Rockville, MD
- $53.00 - $64.81 an hour
- Full-time
- Mid-level
- Databases
- Bachelor's degree
- Travel reimbursement
- Profit sharing
Quick Apply
14d
Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only)
サイネオス・ヘルス —Washington, DC
- Remote
- Microsoft Word
- Microsoft Excel
- Mid-level
- Employee stock purchase plan
- Health insurance
11d
Clinical Program Manager
Guidehouse —Bethesda, MD
- $85,000 - $141,000 a year
- Full-time
- Nursing
- Master's degree
- Databases
- Commuter assistance
- Health savings account
Lead Research Associate - Protocol Specialist - Hybrid
Westat —Bethesda, MD
- $82,000 - $109,000 a year
- Hybrid work
- Background check
- Mid-level
- Office
- Paid parental leave
- Health savings account
14d
Clinical Research Regional Manager
ARIZONA ARTHRITIS & RHEUMATOLOGY ASSOCIATES PC —Rockville, MD
- Clinic
- Bachelor's degree
- Travel
Quick Apply
7d
Project Leader - Oncology & Infectious Diseases
Emmes Group —Rockville, MD
- Full-time
- Remote
- 3 years
- Master's degree
- Analysis skills
- Health insurance
- 401(k)
Project Manager (Public Health)
Ripple Effect —Rockville, MD
- $118,168 - $135,894 a year
- Full-time
- Master's degree
- Business development
- Supervising experience
Quick Apply
Clinical Data Manager
Peers & Partners Inc —Bethesda, MD
- Full-time
- Mid-level
- Office
- Bachelor's degree
Quick Apply
4d
Senior Clinical Data Manager
Supernus Pharmaceuticals Inc —Rockville, MD
- $145,000 - $160,000 a year
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Dental insurance

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MedTech Site Manager 1

IQVIA -
Washington, DC

Apply Now

Job Details

Full-time
$74,500 - $124,100 a year
3 days ago

Benefits

Work from home

Qualifications

Presentation software
Employee relationship building
Clinical audit and monitoring
Presentation creation
Clinical quality assurance standards
Healthcare research

Full Job Description

Washington, United States of America | Full time | Home-based | R1561987

MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and diagnostics industry. Together, we support innovation from concept to commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market optimization. Our teams combine deep therapeutic knowledge with advanced data and technology to help clients make smarter decisions and thrive in the market. Join our team to help shape the future of MedTech.

Position Overview

The In-House Clinical Research Associate/MedTech Site Manager 1 will be a critical team member reporting directly to the Director of Clinical Affairs, to support clinical trial operations for the firm’s clientele. Responsible for management of investigator site and Clinical Research Associate (CRA) activities for assigned studies. The In-House CRA will execute Clinical Affairs functions in accordance with Good Clinical Practice (GCP) guidelines, Standard Operating Procedures (SOPs), and any other applicable regulatory requirements.

Position Responsibilities

Review and approve research and study regulatory documents required for the implementation, monitoring, and evaluation of clinical trials.
Review clinical protocols to ensure collection of data needed for regulatory submissions
Contribute to protocol-specific manuals, plans, and documents as needed.
Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan.
Assist project manager with clinical study planning and management, as required.
Develop and maintain positive relationships both internal and external to project, including clients, team members, and site personnel (PIs, Study coordinators, etc.).
Assist in the identification and recruitment of potential investigators and study sites, as needed.
Ensure Trial Master File is accurate and complete throughout the lifecycle of the project.
Assist with site training for assigned clinical trials.
Assist with site audits and site quality management activities as needed.
Maintain current knowledge of GCP and FDA guidance as it relates to clinical research, as well as current clinical related developments in the assigned therapeutic areas.

Required Qualifications

Bachelor’s degree (B.A./B.S.) in pharmacy, pharmaceutics or a related scientific discipline
2+ years of clinical trial experience. Monitoring experience preferred.
Comprehensive knowledge/ fluency of GCPs and clinical monitoring procedures
Understanding of therapeutic area for assigned clinical projects.
Experience using Electronic Data Capture (EDC) and clinical trial management systems.
Possesses strong written and verbal communication and presentation skills.
Strong research, analytical, critical-thinking and problem solving skills
PC/Technical skills - MS Office, Excel, Word, PowerPoint (Endnote experience is a plus)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $74,500.00 - $124,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

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clinical trial manager jobs in fairfax va

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Position Overview

Position Responsibilities

Review and approve research and study regulatory documents required for the implementation, monitoring, and evaluation of clinical trials.

Review clinical protocols to ensure collection of data needed for regulatory submissions

Contribute to protocol-specific manuals, plans, and documents as needed.

Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan.

Assist project manager with clinical study planning and management, as required.

Develop and maintain positive relationships both internal and external to project, including clients, team members, and site personnel (PIs, Study coordinators, etc.).

Assist in the identification and recruitment of potential investigators and study sites, as needed.

Ensure Trial Master File is accurate and complete throughout the lifecycle of the project.

Assist with site training for assigned clinical trials.

Assist with site audits and site quality management activities as needed.

Maintain current knowledge of GCP and FDA guidance as it relates to clinical research, as well as current clinical related developments in the assigned therapeutic areas.

Required Qualifications

Bachelor’s degree (B.A./B.S.) in pharmacy, pharmaceutics or a related scientific discipline

2+ years of clinical trial experience. Monitoring experience preferred.

Comprehensive knowledge/ fluency of GCPs and clinical monitoring procedures

Understanding of therapeutic area for assigned clinical projects.

Experience using Electronic Data Capture (EDC) and clinical trial management systems.

Possesses strong written and verbal communication and presentation skills.

Strong research, analytical, critical-thinking and problem solving skills

PC/Technical skills - MS Office, Excel, Word, PowerPoint (Endnote experience is a plus)

Where you'll work

Home-based

Culture