Clinical Research Nurse - Ad Hoc

Are you a skilled and compassionate nurse with a passion for clinical research? Join our dynamic team as a Mobile Research Nurse and make a difference in the lives of study patients. We are seeking a dedicated individual with current acute care or homecare experience and phlebotomy skills to work under the guidance of the principal study investigator and nursing management, providing nursing care and supporting clinical research protocols.

As a Mobile Research Nurse, you will play a crucial role in ensuring the successful execution of research studies. You will be responsible for administering investigational medications/products, conducting patient assessments, collecting vital information, and adhering to study protocols with utmost accuracy and ethics. Your expertise and caring nature will help us maintain compliance with each study's protocol and safeguard the well‑being of study patients.

• Accountable for the competent and confident delivery of high‑quality clinical care to patients/participants. Ensure compliance with each study’s protocol by providing thorough review and documentation at each subject study visit.
• Administer investigational medications/products as needed;
  Perform patient assessments to determine presence of side effects; notify Principal Investigator of findings/issues.
• Perform medical tests as outlined in protocol, including, but not limited to: vital signs, specimen collection, electrocardiograms;
  Process specimens and ship specimens per protocol.
• Provide patient education and medical information to study patients to ensure understanding of proper medication dosage, administration, and disease treatment.
• Responsible for adherence to clinical research policies to ensure ethical conduct and protect vulnerable populations.
• Communicate effectively, promoting open and trusting relationships.

• CH‑GCP Certificate
• Graduate from an accredited BSN or Associate Degree in Nursing or Nursing Diploma
• Minimum 2 years’ post‑qualification acute care experience
• BLS certification required
• Experience and knowledge of working in clinical research trials with ICH‑GCP (Good Clinical Practice) Certification – (Training can be provided)
• Good basic IT skills, utilizing mobile devices and Microsoft systems
• Trained in Handling and Transport of Hazardous Substances (training can be provided)
• A flexible schedule is essential
• Unencumbered driver’s license, reliable car
• Competitive pay rates with hourly compensation for travel time and patient interactions.
• Mileage reimbursement for travel expenses.
• Flexible working shifts to accommodate work‑life balance.
• Project‑specific training provided to enhance your skills in clinical research.
• Ongoing training and line management support for professional growth.