Clinical Research Registered Nurse (RN)

Position Overview:
This role is responsible for independently completing clinical trial assignments with precision and within designated timelines. It also includes responsibilities for staff training and development.

Key Functions:

• Uphold PMG’s mission as an Integrated Site Network, delivering exceptional service to clinical trial partners.

• Consistently meet or exceed goals set during quarterly meetings with your supervisor.

• Follow study protocols rigorously while maintaining accurate documentation in line with regulatory standards and internal SOPs.

• Prepare and administer study medications as directed by the Investigator.

• Train site personnel in clinical procedures and CPR/Heartsaver certifications.

Responsibilities:

• Execute technical and clinical tasks required by study protocols, such as venipuncture, specimen processing, vital sign monitoring, EKGs, IV infusions and pump operations, Holter monitoring, pulmonary function testing, allergy testing, pregnancy testing, strep throat screening, injections (IM or SQ), and other protocol-mandated procedures ordered by the investigator.

• Attend investigator meetings, site initiation visits, and coordinator meetings to receive training on drug handling and gain a thorough understanding of protocols and clinical procedures.

• Acquire in-depth knowledge of study drugs, especially those administered via injection or intravenous infusion.

• Monitor patients closely for complications related to drug administration, focusing on injections and IV infusions.

• Maintain detailed dispensing logs, separate from coordinator records, documenting lot numbers, drug vs. placebo status, and information about medication preparation or unblinded mixing personnel.

• Document laboratory results and adverse reactions, promptly informing investigators, sponsors, and the Institutional Review Board of any unexpected or serious events.

• Support other staff members as needed, based on organizational priorities and available time.

• Actively recruit eligible patients and effectively promote clinical trial participation during scheduled recruitment periods each week.

Qualifications:

• Registered Nurse (RN) or a four-year degree (or equivalent) in Biology, Pharmacology, Clinical Research, or a related health field.

• Clinical Research Nurse Coordinators should be certified or actively pursuing certification in cardiopulmonary resuscitation (CPR).

• Some travel may be required, including air travel, to attend investigator meetings.