Clinical Research Nurse

Medasource; Washington (District of Columbia); Presencial; USD 55.000 - 96.000; Jornada completa

Descripción de la vacante

Medasource is seeking an experienced Clinical Research Nurse to support multiple active studies during staffing coverage. The role combines advanced clinical nursing care with research coordination, including participant screening, enrollment, and protocol-driven care.

The ideal candidate is a senior-level nurse with bedside experience and a strong clinical trial background who thrives in a fast-paced research environment and collaborates closely with investigators and care teams.

Formación

• Active RN license in DC and Maryland.
• Minimum of 2 years of clinical trial/clinical research experience.
• Experience with protocol-driven nursing care and infusions.
• Ability to screen and enroll participants against protocol criteria.
• Experience documenting adverse events and regulatory compliance.

Responsabilidades

• Deliver protocol-driven care to research participants (infusions, injections, phlebotomy, assessments).
• Screen, enroll, and determine eligibility for study participants.
• Coordinate visits, data collection, and study documentation across multiple studies.
• Assist with regulatory activities and compliance as needed.
• Collaborate with Principal Investigators and research teams to ensure safety and on-schedule study execution.
• Participate in on-call rotation as needed for select studies.

Conocimientos

Infusions

Phlebotomy

Patient assessments

AE identification/reporting

Clinical research coordination

Screening and enrollment

Collaboration across teams

Educación

Senior-level bedside nursing

Herramientas

GCP knowledge

Descripción del empleo

The client, a provider health system research institute is seeking an experienced Clinical Research Nurse to support multiple active clinical studies during a period of staffing coverage. This role combines advanced clinical nursing care with research coordination responsibilities, including participant screening, enrollment, and protocol-driven nursing care. The ideal candidate is a senior-level nurse with legitimate bedside experience and a strong clinical trial background who works well in a collaborative, fast-paced research environment.

Responsibilities

• Deliver protocol-driven clinical care to research participants, including infusions, injections, phlebotomy, and clinical assessments
• Identify, document, and report adverse events (AEs) in accordance with study protocols, institutional policies, and regulatory requirements
• Screen and enroll potential research participants, verifying eligibility against study inclusion and exclusion criteria
• Perform research coordination activities across multiple studies, including participant visits, data collection, and study documentation
• Support regulatory and compliance activities as needed and where experience allows
• Collaborate closely with Principal Investigators, research staff, and clinical care teams to ensure studies run safely and on schedule
• As available, support after-hours enrollment for select studies, including a sickle cell infusion study where eligible patients presenting to the Emergency Department may be enrolled. Participation in a shared on-call rotation will be compensated for select studies.

Qualifications

• Active Registered Nurse licensure in both the District of Columbia and Maryland
• Senior-level clinical nursing experience with legitimate hands-on bedside nursing experience
• Minimum of 2 years of clinical trial/clinical research experience
• Demonstrated experience with infusions, injections, phlebotomy, and patient assessments
• Experience with AE identification, documentation, and reporting
• Experience with research coordination tasks, including participant screening and enrollment
• Willingness to support bi-weekly on call rotation a needed
• Strong collaboration and interpersonal skills, with the ability to work effectively across clinical and research teams

Preferred Qualifications

• Medical-Surgical (MedSurg) or Progressive Care Unit nursing experience
• Charge nurse or unit lead experience
• Experience supporting regulatory documentation for clinical studies
• Familiarity with GCP and human subjects research requirements