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Contract Clinical Trial Data Transparency Jobs in Raleigh, NC

Biostatistician

Cary, NC · Remote

$60 - $100/hr

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

Biostatistician

Raleigh, NC · Remote

$60 - $100/hr

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

Director of Biostatistics

Cary, NC · Remote

$60 - $100/hr

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

Biostatistician

Durham, NC · Remote

$60 - $100/hr

Source, construct, and curate authentic datasets including trial data, patient records, and ... contract research, hospital, or academic medical contexts. * Demonstrated command of clinical study ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

... Trial Master File, including accurate filing, reconciliation, ongoing review, and execution of ... Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics ...

Showing results 41-60

Contract Clinical Trial Data Transparency information

See Raleigh, NC salary details

$28

$60

$93

How much do contract clinical trial data transparency jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for contract clinical trial data transparency in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What is a contract clinical trial data transparency professional?

A Contract Clinical Trial Data Transparency professional is responsible for ensuring that data from clinical trials are disclosed and reported in accordance with legal, regulatory, and industry standards. They typically work on a contractual basis, helping pharmaceutical or biotech companies comply with data transparency requirements such as posting results on public registries, redacting sensitive information, and supporting data-sharing initiatives. Their work helps promote scientific integrity, protect patient privacy, and maintain public trust in clinical research.

What are some common challenges faced in a contract clinical trial data transparency role, and how are they typically addressed?

Professionals in Contract Clinical Trial Data Transparency often encounter challenges such as navigating complex global regulations, ensuring timely anonymization of sensitive data, and balancing transparency with patient privacy. These challenges are typically addressed by closely collaborating with legal, data management, and clinical teams, as well as staying up-to-date on evolving guidelines from regulatory authorities. Utilizing robust data anonymization tools and standardized processes also helps maintain compliance while meeting transparency requirements.

What are the key skills and qualifications needed to thrive as a contract clinical trial data transparency specialist, and why are they important?

To thrive in Contract Clinical Trial Data Transparency, you need a solid understanding of clinical research processes, regulatory requirements (such as GDPR and FDA guidelines), and strong data management skills, often supported by a degree in life sciences or a related field. Familiarity with data anonymization tools, clinical trial management systems (CTMS), and regulatory submission platforms is typically required. Exceptional attention to detail, strong organizational skills, and effective communication are vital soft skills for managing complex documentation and collaborating across teams. These skills ensure the accurate, compliant, and timely disclosure of clinical trial data, supporting transparency and public trust in research.

What is the difference between Contract Clinical Trial Data Transparency vs Clinical Data Manager?

AspectContract Clinical Trial Data TransparencyClinical Data Manager
Primary FocusEnsuring transparency and accessibility of clinical trial data to stakeholders and the publicManaging and validating clinical trial data for accuracy and completeness
Work EnvironmentContract-based, often project-specific, with collaboration across sponsors, regulators, and CROsIn-house or CRO setting, focused on data collection, cleaning, and database management
Required CredentialsKnowledge of clinical trial regulations, data sharing policies, and industry standardsDegree in life sciences, biostatistics, or related field; experience with clinical data systems

Contract Clinical Trial Data Transparency professionals focus on making clinical data accessible and compliant with transparency regulations, while Clinical Data Managers handle the collection, validation, and management of clinical trial data to ensure quality and integrity. Both roles are essential in the clinical research process but differ in their primary objectives and daily tasks.

What cities near Raleigh, NC are hiring for Contract Clinical Trial Data Transparency jobs?

Cities near Raleigh, NC with the most Contract Clinical Trial Data Transparency job openings:

Infographic showing various Contract Clinical Trial Data Transparency job openings in Raleigh, NC as of July 2026, with employment types broken down into 2% As Needed, 70% Full Time, 20% Part Time, 1% Temporary, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Principal Clinical Scientist (Neurodegenerative)

Danaher

Raleigh, NC • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago


Key responsibilities

  • Design clinical studies and evidence strategies supporting global regulatory submissions across multiple diagnostic modalities.

  • Act as a scientific and clinical liaison with regulatory bodies, key opinion leaders, and external sites to develop protocols, claims, and evidence plans.

  • Partner cross-functionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align clinical programs with product development and market access needs.


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

193rd of 546 rated manufacturers


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

Within Danaher the work our diagnostic businesses do saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

We're accelerating the development of cutting-edge diagnostics to solve some of the world's most pressing health challenges. Across our diagnostics operating companieswe are drivinginnovationthroughpartnerships with top academic institutions and leading players in biopharma and translational research.We're bringing the best minds together toaccelerateinnovation and unlock the full potential of the latest scientific advances. Together, we're expanding access to precision diagnostics for millions of people worldwide - and we're using our unmatched global scale and proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more precise diagnostic results, we're improving treatment options and saving lives.

Learn about theDanaher Business Systemwhich makes everything possible.

Principal Clinical Scientist. This role is responsible for clinical trial strategies within the US and EU regions for Danaher Diagnostics Neurodegenerative program. This role will specifically support Beckman Coulter Diagnostics and Life Sciences, operating companies of Danaher Diagnostics. You will drive strategic study designs, ensuring regulatory compliance, and achieving key milestones for critical clinical studies in these vital markets.

This position is part of the Danaher Diagnostics, Beckman Coulter Inc. organization and will be remote based (can also be onsite in Chaska MN). At Danaher Diagnostics, our vision is to be the leading provider of seamlessly connected diagnostic solutions.

In this role, you will have the opportunity to:

  • Design clinical studies and evidence strategies supporting global regulatory submissions (e.g., FDA 510(k)/PMA, CEIVDR) across multiple diagnostic modalities.
  • Act as a scientific and clinical liaison with regulatory bodies, key opinion leaders, and external sites to develop protocols, claims, and evidence plans.
  • Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align clinical programs with product development and market access needs.
  • Author and review clinical and regulatory documentation-including study reports, technical files, and publications-to support product clearance and commercialization.
  • Build strong internal and external collaborations, mentor junior scientists, and maintain expertise in evolving regulatory standards, clinical guidelines, and diagnostic technologies

The essential requirements of the job include:

  • Bachelor's degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research, specifically with significant experience in US and/or EU trials, or a Master's degree with 12+ years of experience or Doctoral degree with 4+ years of same experience.
  • In-depth understanding of clinical study design and methodology in the diagnostics, medical device, or pharmaceutical industry with products intended for the US and EU markets.
  • Demonstrated ability to identify and solve complex issues in clinical trial conduct and scientific interpretation.
  • Ability to critically review and interpret scientific and clinical trial data, and oversee the scientific aspects of study protocols and reports.
  • Excellent communication (written and verbal) and interpersonal skills for collaborating with cross-functional stakeholders.

It would be a plus if you also possess previous experience in:

  • Experience in study designs for diagnostic technologies (IVD) is highly preferred, specifically for Neurodegenerative Biomarkers.
  • Advanced degree in Science, Healthcare, or Regulatory/Clinical Affairs.
  • Professional certification in Clinical Research (e.g., SoCRA, ACRP).

Danaher Diagnostics, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at danaherbenefitsinfo.com.

This job is also eligible for bonus/incentive pay.

At Beckman Coulter Diagnostics we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Beckman Coulter Diagnostics can provide.

The annual salary range for this role is$120K-$130K.This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984