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Contract Clinical Trial Data Transparency Jobs (NOW HIRING)

R3tek

Clinical Data Analyst

Hillsborough, NJ · On-site

Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...

R3TEK

Clinical Data Analyst

Hillsborough, NJ

Participate in clinical trial data management process. Conduct data analysis, visualization and data modeling based on report design in clinical data models including ambulatory, laboratory ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... data. RESPONSIBILITIES This position is responsible for, but not limited to, the following: * Lead ... Manage clinical site interactions (including assistance with IRB/EC applications, contract ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... data. RESPONSIBILITIES This position is responsible for, but not limited to, the following: * Lead ... Manage clinical site interactions (including assistance with IRB/EC applications, contract ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Partner with Data Management and Biostatistics to oversee clinical data quality metrics, support ... Manage the feasibility, selection, training and evaluation of study personnel (contract and ...

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Contract Clinical Trial Data Transparency information

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

As of Aug 15, 2026, the average hourly pay for contract clinical trial data transparency 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 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 are hiring for Contract Clinical Trial Data Transparency jobs?

Cities with the most Contract Clinical Trial Data Transparency job openings:

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

The most popular types of Clinical Trial Data Transparency jobs are:

What states have the most Contract Clinical Trial Data Transparency jobs?

States with the most job openings for Contract Clinical Trial Data Transparency jobs include:

Contract Clinical Trial Data Transparency jobs near you
Infographic showing various Contract Clinical Trial Data Transparency job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Research Data Entry Specialist

ObjectiveHealth

South Bend, IN • On-site

Full-time

Posted 24 days ago

Job description

Clinical Research Data Entry Specialist (Onsite)
The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research.
ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:
  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care . We want you to join us in doing just that.
Key Responsibilities:
  • Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines.
  • Review source documents and medical records to ensure complete and accurate transcription of participant data.
  • Verify data for accuracy, completeness, and consistency prior to submission.
  • Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel.
  • Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data.
  • Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system.
  • Ensure timely completion of data entry and query resolution to support study milestones and database lock.
  • Maintain accurate study documentation related to data entry activities.
  • Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines.
  • Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed.
  • Maintain confidentiality of participant information and research data.

Qualifications:
  • High school diploma or equivalent.
  • 1+ years of data entry, administrative support, medical office, or related experience.
  • Excellent attention to detail and data accuracy.
  • Strong organizational and time management skills.
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment.
  • Strong written and verbal communication skills.

Requirements
This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant

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