Full-time
Clinical Research Coordinator II - TraCR
$61K/yr – $79K/yr
Bethesda, MDScience & PharmaceuticalPosted 19d ago
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Role overview
Job type
Salary
$61K/yr – $79K/yr
Location
Sector
Posted
19 days ago
Job description
Insider Connection @The Henry M. Jackson Foundation for the Advancement of Military Medicine
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Responsibilities
Assists human subjects’ research activities, to include clinical trial protocol development, study operational procedures and forms development, and study implementation within the NMRC CTC in conjunction with senior staff
Prepares and submits regulatory documents, including scientific and institutional review board submissions
Recruits and screens new subjects for participation in clinical research studies occurring in the NMRC CTC
Reviews new subjects records and screens subjects for eligibility in participation of research protocol(s)
Interviews subjects for protocols and collects and analyzes appropriate data for recruitment purposes, determine subject commitment and obtains informed consent. Educates subjects about the research protocol, their roles in the protocols, and any other vital information
Monitors study progress and identifies and resolves/reports issues, including protocol deviations and non-compliance, to the appropriate parties
Monitors, documents, and reports adverse events and safety concerns in accordance with regulatory and sponsor requirements
Collects, organizes, catalogs, disseminates, and maintains appropriate files of current data. Maintains status reports on all subjects as appropriate
Acts as a liaison between subjects and clinicians and serves as a resource for the subjects
Transcribes and resolves queries of data in case report forms (hardcopy or electronic) and prepares documents, under direction of project heads
Adheres to legal, professional and ethical codes with respect to confidentiality and privacy. Assures that protocol requirements are performed in compliance with Good Clinical Practice and other federal and local regulations
Schedules subjects for appointments and visits. Assists with monitoring audits/visits for protocols
Trains and mentors junior research staff as needed
Travels from their assigned workplace to support protocols at other sites as needed
May perform other duties and responsibilities as assigned or directed by the supervisor. This may include attendance of and participation in required training for role
Benefits
Comprehensive suite of benefits focused on your health and well-being
Medical coverage
Dental coverage
Vision coverage
Health savings
Retirement plans
Glassdoor
3.6
The Henry M.
Bethesda, Maryland, USA
https://www.hjf.org/
Late Stage
Total Funding
$2.2M
Key Investors
BIRD Foundation
TEDCO
Orthopaedic Research and Education Foundation
2025-10-10
Grant
2024-12-11
Grant· $0.9M
2023-10-24
Grant· $1.3M
Leadership Team
John Lowe
President/CEO
Joseph Caravalho
President and CEO
Recent News
Qualifications
Bachelor's Degree in Life Sciences or a related field required
Minimum of 3-5 years experience required
Knowledge of federal and local regulations and policies pertinent to research involving human subjects, to include regulatory submissions
Ability to understand and utilize scientific/medical terminology and research theory in both oral and written communications
Ability to work independently and as part of a team in a fast-paced environment
Excellent interpersonal and computer skills, including experience with MS Office products (MS Outlook, MS Excel, MS Word, MS Teams) and Adobe Professional
Excellent attention to detail
Ability to communicate effectively and to work with individuals of all levels
Holds a valid driver's license
US Citizenship required and the ability to obtain and maintain a T1/Public Trust background check
Lifting: Requires lifting materials up to 25 lbs
Ability to stand or sit at a computer for prolonged periods
Minimum of 3-5 years experience required.
Required skills
Clinical research, Regulatory submissions, Clinical Practice, Scientific/medical terminology, MS Office, Adobe Professional
Experience
3-5 years
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