Clinical Trial Navigator (Temporary)

Javara Inc.; Albany (GA); On-site; USD 42,000 - 62,000; Part time

Job summary

Javara Inc. is seeking a Clinical Trial Navigator (Temporary) in Albany, GA to manage enrollment plans, screen participants, and coordinate study visits.

You will work with investigators, sponsors, and healthcare partners to achieve recruitment targets while upholding safety and regulatory standards. The role requires 1+ year experience in healthcare settings involving clinical functions such as vitals, EKGs, and phlebotomy, with a focus on accurate data capture and sponsor-reporting.

Qualifications

• Associates or Bachelors degree in a related field or equivalent experience.
• Hands-on clinical function experience including vitals, EKGs, and phlebotomy.
• Ability to work in a fast-paced clinical trial environment with attention to safety.

Responsibilities

• Lead enrollment plan for assigned studies and meet recruitment goals.
• Coordinate patient visits, screenings, and informed consent.
• Maintain data integrity and ensure audit-ready study documentation.

Skills

Patient screening

Enrollment planning

Team collaboration

Regulatory knowledge

Data integrity

Education

Associate or Bachelor's degree in related field

Tools

CTMS

EHR/EMR systems

EDC tools

Job description

## Clinical Trial Navigator (Temporary)Applylocations: Albany, GA: Thomasville, GAposted on: Posted Todayjob requisition id: R-100230**Job Description:****Essential 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.**Qualifications:*** 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.**Work Environment:**The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.* This job operates in a professional environment.* The noise level in this work environment is usually light to moderate.**Physical Demands:**The physical demands described here are representative of those that must be met to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.* 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.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.