Clinical Research Coordinator II - Translational Trials Specialist

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.

Bethesda (MD)

On-site

USD 61,000 - 79,000

Full time

4 days ago
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Job summary

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. is seeking a Clinical Research Coordinator II to support translational and clinical research activities within NMRC’s CTC in Bethesda.

The role includes protocol development, regulatory submissions, subject recruitment, data management, adverse event reporting, and mentoring junior staff to advance vaccines, therapeutics, and medical devices for U.S. military personnel.

Qualifications

  • Bachelor's Degree in Life Sciences or related field required.
  • 3–5 years of clinical research experience preferred.
  • Knowledge of federal and local regulations governing human subjects research.
  • Ability to work independently and as part of a team in a fast-paced environment.
  • Proficiency with MS Office and data management tools.

Responsibilities

  • Assist with clinical trial protocol development and study procedures.
  • Prepare regulatory submissions and IRB documentation.
  • Recruit and screen subjects for NMRC CTC studies.
  • Review subject records and determine eligibility for protocols.
  • Educate subjects about protocols and obtain informed consent.
  • Monitor progress, report deviations and adverse events per sponsor requirements.
  • Maintain data files and status reports for subjects.
  • Train and mentor junior staff; travel to support multi-site protocols.

Skills

Regulatory knowledge
Clinical research
Data collection
Interpersonal skills
MS Office
Communication

Education

Bachelor's Degree in Life Sciences

Tools

MS Outlook
MS Excel
MS Word
MS Teams
Adobe Professional

Job description

The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. is seeking a Clinical Research Coordinator II to support translational and clinical research activities within NMRC’s CTC in Bethesda.

The role includes protocol development, regulatory submissions, subject recruitment, data management, adverse event reporting, and mentoring junior staff to advance vaccines, therapeutics, and medical devices for U.S. military personnel.

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