Research Nurse

Ready to combine your nursing expertise with cutting-edge clinical research and help bring tomorrow's treatments to patients today?

R&D Partners is seeking a Research Nurse to support study sites in the coordination of Phase I-IV clinical research studies. This role involves ensuring that studies are conducted in compliance with protocols, standard operating procedures, Good Clinical Practice (GCP), and other applicable guidelines and regulations.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Coordinate clinical research studies under the supervision of the principal investigator.
• Maintain skills, training, and knowledge of current best nursing practices and clinical research topics.
• Safeguard the well-being of study participants and maintain high standards of care.
• Create a safe environment in line with Health and Safety policies.
• Act as a volunteer advocate and address concerns proactively.
• Assist registered and unregistered staff in nursing practices and care delivery.
• Support study conduct by:
• Reviewing study protocols, case report forms (CRFs), and other study documents.
• Participating in project meetings as needed.
• Preparing for clinical set-up, including labeling specimen collection tubes, setting up equipment, and generating volunteer instructions.
• Identifying and obtaining required supplies and equipment.
• Delivering study-specific training materials and troubleshooting study issues.
• Assisting with data quality checks and query resolution.
• Recruit and screen volunteers based on pre-determined criteria.
• Orientate volunteers to the study, including timelines and procedures.
• Administer and manage custody of study drugs according to site SOPs.
• Perform complex clinical procedures such as:
• Vital signs monitoring, phlebotomy, ECG, spirometry, cannulation, and cardiac telemetry monitoring.
• Collect, record, and report clinical data in CRFs.
• Collaborate with study investigators to report adverse events and serious adverse events.
• Work closely with study monitors and allocate time for monitoring activities.

Key Skills and Requirements:

• Strong knowledge of clinical trials and GCP principles.
• Proficiency in MS Windows and Office applications.
• Effective written and verbal communication skills in English.
• Excellent interpersonal and problem-solving skills.
• Strong organizational skills and attention to detail.
• Ability to establish and maintain effective working relationships with colleagues and clients.

Education and Experience:

• Bachelor's degree or equivalent in Nursing with at least 1 year of relevant experience.
• Current active nursing license in the region where the site is located.
• Applicable certifications and licenses as required by regulatory bodies.

Physical Requirements:

• Freuent use of telephone and face-to-face communication.
• Use of keyboard requiring repetitive motion of fingers.
• Regular mobility around the facility.

About the Role

The primary focus of this position is to perform study coordination, administrative tasks, and patient care, including:

• Conducting vital signs checks, blood draws, and administration of investigational products (IP).
• Collecting, recording, and reporting clinical data.
• Assisting with study enrollment through recruitment and screening.
• Preparing for clinical set-up and ensuring data quality and accuracy.

For more information, please contact Mandi Cakwe.

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