Clinical Trial Navigator I

Javara•Mankato, MN

5d•Onsite

About The Position

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. This role is essential for improving the patient's experience in clinical trials while ensuring safety and scientific integrity. The Clinical Trial Navigator will operate as the lead for assigned studies, focusing on enrollment strategies, patient retention, and accurate data management. They will also coordinate patient visits, perform clinical skills, and educate the research team and healthcare staff on study procedures.

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.
Drug screen and background check required.

Responsibilities

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 Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.
Additional tasks as assigned.