1

Clinical Trial Transparency Associate Jobs in Georgia

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 ...

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 ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

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 ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

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 ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Operate as the lead Clinical Trial Navigator for at least one clinical study by owning the ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Operate as the lead Clinical Trial Navigator for at least one clinical study by owning the ... Associates or Bachelor's Degree in related field or equivalent industry experience. * 1+ years ...

Clinical Affairs Scientist

Turin, GA · On-site +1

$105K - $197K/yr

The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...

Our associates are involved in every stage of diagnostics, from ideation to development and ... This role is responsible for clinical trial strategies within the US and EU regions for Danaher ...

New

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their ...

next page

Showing results 1-20

Clinical Trial Transparency Associate information

See Georgia salary details

$14

$33

$59

How much do clinical trial transparency associate jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical trial transparency associate in Georgia is $33.76, according to ZipRecruiter salary data. Most workers in this role earn between $27.21 and $37.16 per hour, depending on experience, location, and employer.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are the most commonly searched types of Clinical Trial Transparency jobs in Georgia?

The most popular types of Clinical Trial Transparency jobs in Georgia are:

What are popular job titles related to Clinical Trial Transparency Associate jobs in Georgia?

For Clinical Trial Transparency Associate jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Transparency Associate jobs in Georgia look for?

The top searched job categories for Clinical Trial Transparency Associate jobs in Georgia are:

What cities in Georgia are hiring for Clinical Trial Transparency Associate jobs?

Cities in Georgia with the most Clinical Trial Transparency Associate job openings:

Clinical Trial Navigator I

Javara Inc.

Albany, GA • On-site

Other

Re-posted 7 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.