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Clinical Trial Transparency Jobs (NOW HIRING)

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

  • Medical

  • Retirement

  • PTO

Our mission is to bring innovation to clinical trial execution through passion, transparency, co-active communication, and integrity, to facilitate the successful development of life-changing ...

Xogene Services Llc

Enterprise Account Executive

New York, NY · On-site

$70K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

At Xogene, we're revolutionizing the future of clinical trial transparency through AI-powered solutions. Join our team of experts who are transforming how leading pharmaceutical and life sciences ...

MyOme

Senior Clinical Trial Manager

San Francisco, CA

$145K - $185K/yr

The Senior Clinical Trial Manager is a key contributor to MyOme's clinical evidence generation ... Value humility, transparency, and collaborative problem-solving * Thrive in fast-moving, dynamic ...

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Biogen

Sr. Manager - Clinical Trial Lead

Cambridge, MA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Supports the development of comprehensive clinical trial budgets that accurately reflect the costs ... Collaborates with Procurement to ensure FMV transparency, regularly monitoring the budget to ...

Biogen

Sr. Manager - Clinical Trial Lead

Cambridge, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... transparency, regularly monitoring the budget to identify potential overspending and addressing ... department clinical trial outsourcing models; provides feedback via appropriate channels for ...

Vanguard Clinical

Clinical Operations Specialist (Pool)

CA · Remote

  • Medical

  • Retirement

  • PTO

Our mission is to bring innovation to clinical trial execution through passion, transparency, co-active communication, and integrity, to facilitate the successful development of life-changing ...

ImmunityBio, Inc.

Agency Temporary, Contracts Counsel

$97.35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Proven ability to handle a wide range of general corporate and commercial contracts beyond the clinical context. * Integrity and ethics, adaptability, innovation/creativity * Analytical thinking ...

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Clinical Trial Transparency information

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How much do clinical trial transparency jobs pay per hour?

As of Aug 14, 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?

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 a 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.

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Clinical Trial Transparency jobs near you
Infographic showing various Clinical Trial Transparency job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% 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 Associate/Senior Clinical Trial Associate

Crescent Biopharma

Waltham, MA • On-site

$108K - $132K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago

Job description

Crescent Biopharma's vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company's clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.
We are seeking a CTA/Senior CTA who will work with the Clinical Study Lead and Director of Clinical Operations to support the conduct of clinical trials. You will partner with the Clinical Study Lead to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.
You may independently manage components of clinical studies, including but not limited to vendor oversight, budgets, responsibility for a subset of sites or countries, or phases of the trial (startup period, for example), with oversight.
Responsibilities
  • Support the Clinical Study Lead and Clinical Operations team in the day-to-day operational activities of clinical trials to ensure study objectives, timelines, quality standards, and regulatory requirements are met.
  • Support oversight of CROs, vendors, and investigator sites, including review of monitoring visit reports, site communications, and follow-up on study-related actions and issues.
  • Maintain study tracking tools for key study documentation (e.g., Form FDA 1572) and operational activities, including site activation, enrollment, monitoring visit status, IRB/EC approvals, safety letter distribution, training compliance, and study milestones.
  • Support Trial Master File (eTMF) activities, including document collection, filing, reconciliation, quality control reviews, and inspection readiness efforts.
  • Support preparation of study agendas, meeting minutes, action item logs, and study status reports while ensuring effective communication across internal teams, CROs, vendors, and investigator sites.
  • Collaborate cross-functionally with Regulatory Affairs, Clinical Supplies, Data Management, Safety, Quality, and other functional areas to support study deliverables and timelines.
  • Manage study team training records and ensure compliance with applicable SOPs, regulations, study requirements, and company policies.
  • Manage system access requests for study team and site personnel, as needed.
  • Communicate and escalate study risks, protocol deviations, operational challenges, and other study-related issues as appropriate.

Education & Experience
  • Bachelor's degree in scientific or related field with 2+ years of experience in Clinical Operations, clinical research or healthcare, or equivalent experience
  • Knowledge of FDA regulatory requirements and ICH/GCP guidelines essential
  • Demonstrated efficiency in partnering with CROs and vendors
  • Computer proficiency (Word, Excel, PowerPoint, Project)
  • Works proactively and efficiently in a fast-paced, high change environment
  • Must have excellent interpersonal, written and verbal communication skills
  • Ability to interact well with various team members and provide value added support to project
  • Outstanding organization skills
  • Strong analytical, strategic thinking, and problem-solving skills.
  • Ability to quickly learn new tools, systems, and processes to improve efficiency

What We Offer
  • Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment
  • Competitive compensation, including base salary, performance bonus, and equity
  • 100% employer-paid benefits package
  • Flexible PTO
  • Two, one-week company-wide shutdowns each year
  • A commitment to your professional development, with access to resources, mentorship, and growth opportunities

Salary Range
The anticipated salary range for this position is $108,000 to $132,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.
Additional Description for Pay Transparency:
The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company's savings plan (401(k)). This position is eligible to participate in the Company's long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation - Unlimited PTO; Sick time - 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave - 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - https://www.crescentbiopharma.com/careers/#benefits
Please note:
Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.
Please note, Crescent does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between Crescent and the agency. Crescent will not pay any fees related to unsolicited resumes.
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