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Temporary Clinical Trial Navigator Jobs (NOW HIRING)

Clinical Trial Navigator II As a Clinical Trial Navigator II with Javara, you will be responsible for the coordination and administration of clinical trials and report to the Manager of Site ...

Position Summary The Clinical Trial Navigator (CTN) is a Registered Nurse who serves as a key liaison between Caris Life Sciences and physicians who order Caris molecular profiling. Leveraging ...

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Clinical Trial Navigator (Temporary)

Albany, GA · On-site

$30.75 - $42/hr

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 ...

Clinical Trial Navigator (Temporary)

Albany, GA · On-site

$30.75 - $42/hr

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 ...

Clinical Trial Navigator (Temporary)

Thomasville, GA · On-site

$27.25 - $37/hr

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 ...

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 ...

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 ...

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 ...

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 ...

Operate as the lead Clinical Trial Navigator for multiple clinical studies, dependent upon site-specific study needs such as study complexity and enrollment goal volume, by owning the enrollment plan ...

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 ...

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 ...

Operate as the lead Clinical Trial Navigator for multiple clinical studies, dependent upon site-specific study needs such as study complexity and enrollment goal volume, by owning the enrollment plan ...

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Temporary Clinical Trial Navigator information

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How much do temporary clinical trial navigator jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for temporary clinical trial navigator in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Trial Navigator vs Clinical Research Coordinator?

AspectTemporary Clinical Trial NavigatorClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentTemporary positions in clinical trial sites, hospitals, or research organizationsPermanent or temporary roles in research sites, hospitals, or academic institutions
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for short-term trial supportEmployed by research institutions, hospitals, and pharma companies for ongoing trial management

The main difference is that a Temporary Clinical Trial Navigator is a short-term, project-based role focusing on guiding patients and coordinating trial activities temporarily. In contrast, a Clinical Research Coordinator typically holds a more permanent position responsible for managing all aspects of clinical trials on an ongoing basis.

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Infographic showing various Temporary Clinical Trial Navigator job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Navigator I

Albany, GA • On-site

Javara Inc.
Scientific Research and Development Services • 51 - 200 employees

Other

Re-posted 8 days ago


Job description

Clinical Trial Navigator II

As a Clinical Trial Navigator II 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.

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 multiple clinical studies, dependent upon site-specific study needs such as study complexity and enrollment goal volume, by owning the enrollment plan and strategies to achieve and exceed expectations. May serve as a lead CTN across Javara for a single study, providing support and guidance to other assigned CTNs.
  • Execute the enrollment plan of assigned studies to meet requirement goals by identifying and contacting potential participants and screening to enroll into suitable studies.
  • Support enrollment goals by contributing to patient retention strategies and building relationships within local communities.
  • Participate in developing creative approaches to patient recruitment and retention strategies, including participating in community engagement.
  • 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.
  • Support continuous improvement by assisting in implementing updated processes or procedures intended to improve the experience of internal and external stakeholders.
  • 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 on the continuous impact of your role on study and site success.
  • 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.
  • 2+ years of experience in clinical research 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.

Pre-Employment Screening: Drug screen and background check required.

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.

Equal Employment Opportunity Statement: Javara provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.