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Research Nurse Coordinator
2 months ago
Hackensack Meridian Health is seeking a highly skilled Clinical Research Nurse to join our team. As a key member of our research team, you will be responsible for coordinating and overseeing clinical research operations for all assigned clinical trials.
Key Responsibilities- Protocol Management: Assist the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
- Regulatory Compliance: Assure that all protocol revisions, informed consents, continuing reviews, serious adverse events are submitted to the appropriate IRB of record in a timely manner.
- Liaison and Communication: Act as liaison between principal investigators and sub-investigators on all regulatory issues and changes within the protocol.
- Study Feasibility: In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
- Study Budgeting: Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. Finalizes budget draft with budget coordinator.
- Patient Recruitment: Recruits and evaluates potential study patients, and works with clinical research coordinator to schedule required appointments and interviews.
- Study Coordination: Coordinates research activities not limited to: scheduling laboratory tests, radiology testing and other medical exams.
- Documentation and Reporting: Maintains accurate, complete, up-to-date records on each patient participating in a clinical trial protocol. Ensures study patient's clinical trial related activities are billed appropriately and reconciles drug study account records with research finance personnel.
- Monitor Site Visits: Prepares and assists for sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit.
- Education and Training: Provides education to all departments and clinical areas where study is performed. Attends research meetings and conferences as required.
- Education: BSN required. (Note: this applies to team members hired or transferred on or after March 31, 2024. Team members hired or transferred prior to March 31, 2024 require a minimum of an associate in Nursing or diploma of Nursing degree.)
- Experience: Minimum of 3 years clinical nursing experience or 1 year of clinical nursing experience with an additional 2 years of clinical research experience.
- Certifications: NJ State Professional Registered Nurse License. BLS/CPR certification by American Heart Association is required within 60 days of hire.
