Research Nurse

Saratoga Medical Center • Bethesda, MD

3d • Onsite

About The Position

Saratoga Medical has an exciting opportunity for a Research Nurse in Bethesda, MD. This is a great full-time opportunity with a 40-hour work week schedule, Monday to Friday, excluding Federal holidays. The role involves recruiting and screening patients for clinical research protocols and trials, performing physical assessments, collecting medical histories, and assessing patient eligibility. The nurse will also obtain informed consent, support IRB submissions, document and report adverse events, perform research data entry, and interpret clinical data. Collaboration with physicians, principal investigators, and other healthcare professionals is key, as is assisting in developing new protocols and training new staff. Maintaining accurate records, protecting participant confidentiality and safety, and adhering to NIH, NIDDK, institutional, and applicable clinical research policies and procedures are essential.

Requirements

• Recruit and screen patients for clinical research protocols and trials.
• Perform physical assessments and collect comprehensive medical histories.
• Assess patient eligibility in accordance with study-specific inclusion and exclusion criteria.
• Obtain informed consent and maintain appropriate participant documentation.
• Support IRB submissions, regulatory reporting, annual reviews, and protocol compliance.
• Document and report adverse events (AEs), protocol deviations, and other reportable occurrences.
• Perform research data entry, database maintenance, and data quality checks.
• Interpret clinical data and research findings and communicate relevant information to investigators and the research team.
• Collaborate with physicians, principal investigators, research coordinators, and other healthcare professionals.
• Assist in developing and implementing new clinical research protocols.
• Train and mentor new staff on research procedures and protocol requirements.
• Maintain accurate clinical and research records while protecting participant confidentiality and safety.
• Follow NIH, NIDDK, institutional, and applicable clinical research policies and procedures.

Responsibilities

• Recruit and screen patients for clinical research protocols and trials.
• Perform physical assessments and collect comprehensive medical histories.
• Assess patient eligibility in accordance with study-specific inclusion and exclusion criteria.
• Obtain informed consent and maintain appropriate participant documentation.
• Support IRB submissions, regulatory reporting, annual reviews, and protocol compliance.
• Document and report adverse events (AEs), protocol deviations, and other reportable occurrences.
• Perform research data entry, database maintenance, and data quality checks.
• Interpret clinical data and research findings and communicate relevant information to investigators and the research team.
• Collaborate with physicians, principal investigators, research coordinators, and other healthcare professionals.
• Assist in developing and implementing new clinical research protocols.
• Train and mentor new staff on research procedures and protocol requirements.
• Maintain accurate clinical and research records while protecting participant confidentiality and safety.
• Follow NIH, NIDDK, institutional, and applicable clinical research policies and procedures.

Benefits

• competitive rate
• paid time off
• benefit options

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed