Clinical Trial Navigator I (PRN)
About The Position
As a PRN Clinical Trial Navigator I with Javara, you will be responsible for the coordination and administration of clinical trials and report to the Manager of Site Operations and the Principal Investigator or designee. You will be a critical member of our organization and contribute to patient enrollment efforts within a variety of clinical trials. With a guiding principle of research participant safety, you will implement and coordinate research study procedures for the successful management of clinical trials. Javara is an integrated research organization (IRO) that advances value by integrating clinical research within the healthcare ecosystem. Javara brings better outcomes for patient centered care, better economic results, improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.
Requirements
- Associates or Bachelor’s Degree in related field or equivalent industry experience.
- 1+ years’ experience in healthcare or a related field that includes hands-on application of clinical functions such as obtaining vitals, EKGs, and phlebotomy.
Responsibilities
- Seek to improve the patient’s experience, never compromising on safety.
- Provide excellent customer service to patients and participants, healthcare partner and practice stat investigators, sponsors, and vendors.
- Operate as the lead Clinical Trial Navigator for at least one clinical study by owning the enrollment plan and strategies to achieve and exceed expectations.
- Execute the enrollment plan of assigned studies to meet requirement goals by identifying and contacting potential participants and screening to enroll into suitable studies.
- Build effective working relationships with colleagues, patients, investigators, and other internal and external partners on clinical trials.
- Support enrollment goals by contributing to patient retention strategies and building relationships within local communities.
- Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor’s case report form, and timely query resolution.
- Ensure study documentation is up to date and audit ready, including reporting of adverse events and deviations with investigational products.
- Adhere to all Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), protocols, OSHA, proper PPE usage and other regulatory authority requirements.
- Conduct and document the informed consent process.
- Inform and educate the research team and healthcare system staff regarding study related procedures including IP dosing and monitoring requirements.
- Coordinate and schedule patient visits and conduct visits per protocols.
- Appropriately communicate and escalate to support responsiveness and resolution with our healthcare partners and other external stakeholders.
- Perform clinical and laboratory skills such as therapeutic area specifics, obtaining vitals, phlebotomy, EKGs, and collecting, processing, and shipping bodily samples.
- Demonstrate thoughtfulness around the immediate impact of your role on clinical trials.
- Demonstrate our Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.
- Additional tasks as assigned.
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What This Job Offers
Career Level
Entry Level
Education Level
Associate degree
