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Clinical Trial Transparency Jobs (NOW HIRING)

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Boston, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Boston, MA

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Watertown, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

Adams Clinical

Clinician, Rater

Boston, MA · On-site

$90K - $120K/yr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... A culture of respect, transparency, and continuous improvement * Opportunities for professional ...

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Clinical Trial Transparency information

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How much do clinical trial transparency jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for clinical trial 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 Clinical Trial Transparency job?

A Clinical Trial Transparency job involves ensuring that information about clinical trials is publicly disclosed in compliance with global regulations and transparency policies. Professionals in this role manage the registration of trials on public databases, oversee the timely reporting of results, and ensure adherence to ethical and legal requirements. They collaborate with regulatory teams, medical writers, and legal departments to promote data accessibility and public trust in clinical research.

What are the main responsibilities in a Clinical Trial Transparency role?

In a Clinical Trial Transparency role, your primary responsibilities include preparing and submitting clinical trial data and documents to public registries, ensuring compliance with global regulations, and responding to transparency-related inquiries from regulatory authorities. You’ll work closely with clinical teams, regulatory affairs, and medical writing staff to gather accurate data and ensure timely disclosures. The role often involves managing multiple projects simultaneously, staying updated on evolving disclosure regulations, and supporting audits or inspections. This position is essential in promoting openness, protecting patient privacy, and maintaining the integrity of clinical research.

What are the key skills and qualifications needed to thrive in the Clinical Trial Transparency position, and why are they important?

Excelling in Clinical Trial Transparency requires a comprehensive understanding of clinical research protocols, regulatory compliance (such as FDA, EMA, and ICMJE requirements), and strong project management abilities. Familiarity with disclosure platforms (e.g., ClinicalTrials.gov, EudraCT), data anonymization tools, and relevant certifications like a GCP (Good Clinical Practice) certificate are highly valuable. Attention to detail, effective communication, and stakeholder management are crucial soft skills for success in this role. These capabilities ensure accurate, timely, and compliant disclosure of trial information, which is critical for regulatory approval and upholding public trust.

More about Clinical Trial Transparency jobs
What cities are hiring for Clinical Trial Transparency jobs? Cities with the most Clinical Trial Transparency job openings:
What are the most commonly searched types of Clinical Trial Transparency jobs? The most popular types of Clinical Trial Transparency jobs are:
What states have the most Clinical Trial Transparency jobs? States with the most job openings for Clinical Trial Transparency jobs include:
What job categories do people searching Clinical Trial Transparency jobs look for? The top searched job categories for Clinical Trial Transparency jobs are:
Clinical Trial Transparency jobs near you
Infographic showing various Clinical Trial Transparency job openings in the United States as of June 2026, with employment types broken down into 3% Locum Tenens, 60% Full Time, 5% Part Time, and 32% Contract. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
Senior Manager, Clinical Supply Chain

Senior Manager, Clinical Supply Chain

Skyhawk Therapeutics

Waltham, MA • On-site

$120K - $160K/yr

Other

Posted 23 days ago

Job description

Senior Manager, Clinical Supply Chain

Reporting to the Senior Director of Clinical Supply Chain, the Clinical Supply Chain Senior Manager is responsible for the management and oversight of end-to-end clinical supply chain activity for assigned clinical protocols. This position works closely with key stake holders including Clinical Operations, CMC, Quality Assurance, Regulatory Affairs, Contract Manufacturing Operations (CMO's), and Contract Research Operations (CRO's) to ensure seamless supply of Clinical Trial Material. Some key areas of management/oversight include forecasting, packaging, labeling, distribution, inventory management, financial planning/ budgeting, and vendor oversight.

Responsibilities (including, but not limited to):

  • Manage end-to-end clinical supply chain activity across assigned protocols including forecasting, packaging, labeling, distribution, inventory management, and destruction for global clinical trials
  • Ensure on time delivery of clinical trial material to clinical sites while maintaining cost-effectiveness and compliance with regulatory requirements
  • Drive label creation and approval process, including translations and regulatory requirements
  • Partner with Clinical Operations to align clinical supply needs and timelines
  • Develop supply strategies to maximize supply efficiency and minimize waste
  • Design and actively manage supply & demand forecasts in our home-grown optimization tool
  • Monitor enrollment activity and inventory levels at depots and sites through the life of the trial
  • Identify potential supply risks, and develop risk mitigation plans as necessary
  • Support Interactive Response Technology (IRT) development, user acceptance testing (UAT), and system oversight, as well as utilize the system to actively manage clinical trial material
  • Support return and destruction of clinical trial material for assigned protocols
  • Prepare and manage budget for assigned protocols utilizing budget, planning, and allocation tools
  • Communicate clinical supply requirements to CMC and ensure seamless coordination of demand and supply
  • Oversee third party vendors for assigned protocols to ensure alignment and delivery on project requirements and ensure service levels, quality, and timelines meet Dragonfly standards
  • Review clinical documents to ensure alignment with clinical supply chain activity
  • Provide support for regulatory filings as needed (IND, CTA, IMPD updates, etc)
  • Ensure adherence to applicable regulations including FDA, EMA, ICH, GMP, GxP, and Dragonfly policies and procedures

Education / Skills / Experience Required:

  • Bachelor's degree in Life Sciences or Supply Chain Management
  • 5+ years clinical supply chain experience
  • Strong understanding of end-to-end clinical supply chain activity
  • Experience with supply/demand forecasting
  • Experience with IxRS/ IRT/ RTSM system set-up and management
  • Strong understanding of GxP
  • Demonstrated ability to adapt to change through identifying new strategies and tactics
  • Strong attention to detail
  • Excellent communication, collaboration, and influencing skills
  • Ability to multi-task and manage complex challenges
  • Proficient knowledge of MS Office (Excel, PowerPoint, Visio, Project, etc

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Program Manager is $120,000-160,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.

 

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