Clinical Trial Navigator I

Javara; Savannah (GA); On-site; USD 40,000 - 55,000; Full time

Job summary

A leading healthcare organization in Savannah, Georgia is seeking a Clinical Trial Navigator I. This position involves enhancing the patient experience while ensuring safety and excellence in service delivery. The ideal candidate will lead clinical studies, manage enrollment, and have hands-on clinical skills. Applicants should possess an Associate's or Bachelor's degree in a related field and have at least one year of experience in healthcare, making this an excellent opportunity for those looking to advance their career in clinical trials.

Qualifications

• 1+ years’ experience in healthcare or related field with hands-on clinical functions.
• Ability to perform clinical skills such as phlebotomy, EKGs, and obtaining vitals.

Responsibilities

• Improve patient experience while ensuring safety.
• Lead Clinical Trial Navigator for assigned studies.
• Build working relationships with colleagues and healthcare partners.

Skills

Customer service

Communication

Clinical skills

Relationship building

Education

Associate’s or Bachelor’s Degree in a related field

Job description

Clinical Trial Navigator I – Javara

Join to apply for the Clinical Trial Navigator I role at Javara.

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 elevate 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.

Qualifications

• Associate’s or Bachelor’s Degree in a 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.

Work Environment

• This job operates in a professional environment.
• The noise level in this work environment is usually light to moderate.

Physical Demands

• The employee will regularly use hands to reach, handle or feel objects, tools, or controls and talk and hear.
• The employee may frequently stand, walk and sit.
• The employee may occasionally lift and/or move up to 25 pounds.
• Specific vision abilities required include close vision, distance vision and the ability to adjust focus.

Travel

This position may require up to 30% travel regionally but may occasionally include travel to other regions or Javara headquarters in Winston‑Salem, NC.

Pre‑Employment Screening

Drug screen and background check required.

Additional Information

This job description covers the most essential functions of this position and is not designed to contain a comprehensive listing of activities, duties or responsibilities that are required of the employee in this job. Duties, responsibilities, and activities may change at any time with or without notice.