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Clinical Research Nurse Supervisor

Medical

Full Time

Danbury, US

Posted 2 weeks ago

About the Job

Salary - $130000 - $160000/Year

Supervisor Clinical Research Operations

The CRN Supervisor supports HQ’s Division of Oncology Clinical Research by providing day-to-day oversight of the research staff (CRCs, CRNs)’s clinical trial activities from study start-up to study closure including study surveillance and enrollment, study research patient visits, data collection and entry, and regulatory document collection. This will include serving as a coordinator on trials to support the function of the department. Supervises day-to-day activities for Clinical Research Nurses and Clinical Research Coordinators

Responsibilities:

· Responsible for the complete coordination of assigned clinical research protocols from federal, foundation and industry sponsors in compliance with good clinical practice and applicable federal research regulations.

· Supports Investigators, with the initiation of research protocols, including assisting departmental management in budget and coverage analyses, helping Investigators in training the staff as appropriate, and overseeing the coordinator’s regulatory submissions, etc.

· Provides support to the management of clinical research databases including departmental-approved clinical trial management software and study-specific databases from study sponsors (Electronic Data Capture systems).

· Ensures that accurate and timely communication is facilitated, including between the sponsor and Oncology research division and any regulatory bodies, such as the FDA.

· Conducts weekly meetings with the research staff to ensure all research-related timelines are maintained, especially with respect to data submission, regulatory submissions, and recruitment campaigns.

· Clinical duties include, conducting protocol-specific research tasks within the scope of practice (e.g. phlebotomy, EKG, blood pressure, etc.) as well as a limited role in non-research clinical nursing duties as necessary.

· Oversee day-to-day operations within the span of control, resolving problems as necessary, and ensuring that operations are efficient, compliant, safe, and of the highest possible quality. Optimize management structures and workflows within the span of control to continually improve quality and efficiency.

· Comply with all company and affiliate policies and ensure compliance with all applicable laws and regulations.

· Maintain contemporary professional knowledge and education.

· Demonstrates regular, reliable, and predictable attendance.

· Performs other duties as required.

Requirements:

· Bachelor’s Degree, Master’s Degree a plus.

· Registered Nurse (RN) or Licensed Practical Nurse (LPN). If no NYS then must get a transfer.

· 2+ years’ experience as a nurse or nursing clinical research coordinator or nurse.

· 1+ years of lead, charge, managerial, or supervisory experience.

· MS Excel, Windows, PowerPoint.

· Proven ability to work independently

· Current Basic Life Support (BLS) certification.

· Clinical Research Coordinator (ACRP-CP or SoCRA-CCRP) certification or equivalent experience a plus

Posted 2 weeks ago

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