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Contract Clinical Trial Data Transparency Jobs (NOW HIRING)

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Negotiate master service agreements, work orders, contracts, and amendments for sites/vendors ... Work closely with Data Management to ensure ongoing data cleaning including review of data ...

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 ...

Skyhawk Therapeutics

Clinical Trial Manager

Waltham, MA · On-site

$140K - $200K/yr

... and managing to contracts and budgets * Management of study training for study team ... transparency and equitable compensation practices. The base salary range for the Clinical Trial ...

Kumquat Biosciences Inc

Clinical Trial Manager (CTM)

$140K - $155K/yr

Manage trial budgets, contracts, and vendor relationships. * Collaborate with investigators ... Oversee vendors and investigative sites in the collection and management of clinical data to ...

New

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 · 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 ...

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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 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 Trial Manager (CTM)

Kumquat Biosciences Inc

San Diego, CA • On-site

$140K - $155K/yr

Full-time

Posted 3 days ago

New

Job description

Description:

Summary:


We are seeking an experienced and results-driven Clinical Trial Manager to join our team at Kumquat Biosciences. As a Clinical Trial Manager, you will play a pivotal role in planning, executing, and overseeing oncology clinical trials. You will be responsible for managing cross-functional teams, ensuring study milestones are met, and that trials are conducted in compliance with regulatory guidelines and company protocols.


Key Responsibilities:


  • Perform the day-to-day management of early phase clinical trials or support the study lead(s) on one or more complex global clinical trials.
  • Develop and execute clinical trial plans, including study timelines, budgets, and resource allocation.
  • Manage trial budgets, contracts, and vendor relationships.
  • Collaborate with investigators, clinical sites, and key opinion leaders to ensure successful trial execution.
  • Ensure the timely initiation, monitoring, and close-out of clinical trial sites, including the selection of qualified investigative sites.
  • Oversee patient recruitment and retention strategies, ensuring trial objectives are met.
  • Oversee vendors and investigative sites in the collection and management of clinical data to fulfill study objectives.
  • Proactively identify and mitigate risks and challenges throughout the course of the trial.
  • Ensure strict compliance with Good Clinical Practice (GCP) guidelines and relevant regulations.
  • Prepare for and manage audits and inspections by regulatory authorities.
Requirements:
  • Bachelor's degree in a related field (Life Sciences, Nursing, etc.), or equivalent experience.
  • 6+ years of clinical operations experience or related drug development with 2+ years at a sponsor company.
  • Vendor/clinical service provider management experience required.
  • In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical research.
  • Strong clinical study execution, leadership, and project management skills required.
  • Demonstrated experience in data cleaning and management to support study objectives and data deliverables.
  • Excellent communication, collaboration, and problem-solving abilities.
  • Proficiency in using Microsoft Office applications, clinical trial management systems, and electronic data capture systems.
  • Willingness to travel to investigational sites as required.
  • Familiarity with early phase clinical trial protocols and procedures a plus.

Salary Description: $140k-$155k