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Contract Clinical Trial Data Transparency Jobs in Raleigh, NC

Hays

Clinical Trial Coordinator

Chapel Hill, NC · On-site

It's a 6month of contract (With the higher possibility of full-time conversion and Extension) Key ... Enter and review data in EDC, CRF, and EMR systems. * Support monitoring visits, audits, and ...

IQVIA

Clinical Trial Rater

Durham, NC · Remote

Clinical Specialist Start: immediate Contract based About IQVIA IQVIA is a global leader in ... Our mission is to combine data science and human expertise to transform healthcare worldwide. We ...

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Clinical Specialist Start: immediate Contract based About IQVIA IQVIA is a global leader in ... Our mission is to combine data science and human expertise to transform healthcare worldwide. We ...

Aerogen

Clinical Trial Manager

Morrisville, NC · On-site

$100 - $125/hr

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... The CTM oversees vendor management, monitors subject safety and data collection, and ensures ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC · On-site

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

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

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

Allucent

Clinical Trial Lead

Cary, NC · On-site

$150 - $200/hr

The CTLis responsible forcoordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelinesand withquality.

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

The CTLis responsible forcoordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelinesand withquality.

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.

Allucent

Clinical Trial Lead

Cary, NC · Remote

The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Lead interdisciplinary core trial teams (e.g., data management, statistics, pharmacokinetics, clinical operations) and facilitate Trial Oversight Meetings. Collaborate cross-functionally to support ...

IQVIA

EDC Clinical Trial Designer

Durham, NC

$68K - $171K/yr

Job Summary The EDC Clinical Trial Designer will create high quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing ...

IQVIA, Inc.

EDC Clinical Trial Designer

Durham, NC · On-site

$68K - $171K/yr

Job Summary The EDC Clinical Trial Designer will create high quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing ...

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All JobsContract Clinical Trial Data Transparency JobsContract Clinical Trial Data Transparency Jobs in Raleigh, NC

Contract Clinical Trial Data Transparency information

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

As of Sep 7, 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:

Contract Clinical Trial Data Transparency jobs near you
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.

Clinical Trial Coordinator

Hays

Chapel Hill, NC • On-site

Other

Posted 12 days ago

Job description

About the Role

Hays is partnering with a leading global pharmaceutical organization to hire a Clinical Trial Coordinator to support the day-to-day management of clinical research studies. This role will work closely with investigators, patients, and clinical teams to ensure studies are conducted safely, efficiently, and in compliance with regulatory requirements.

It's a 6month of contract (With the higher possibility of full-time conversion and Extension)


Key Responsibilities:

  • Coordinate clinical trials from start-up through closeout.
  • Recruit, screen, and enroll study participants.
  • Manage informed consent and study visits.
  • Maintain study documentation and regulatory records.
  • Enter and review data in EDC, CRF, and EMR systems.
  • Support monitoring visits, audits, and compliance activities.
  • Collaborate with investigators, sponsors, and research staff.


Qualifications:

  • Bachelor's degree in a scientific, healthcare, or related field.
  • 1+ year of clinical research experience.
  • Knowledge of ICH-GCP and FDA regulations.
  • Experience with patient-facing research activities, data management, and clinical trial documentation.
  • Strong organizational, communication, and multitasking skills.
  • Oncology clinical research experience.


Apply