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Clinical Trial Transparency Associate Jobs (NOW HIRING)

Biogen

Senior Clinical Trial Transparency Specialist

$116K - $155K/yr

About This Role The Senior Clinical Trial Transparency Specialist leads clinical trial transparency activities for assigned studies, helping ensure that trial registration and results information are ...

Biogen

Senior Clinical Trial Transparency Specialist

$116K - $155K/yr

About This Role The Senior Clinical Trial Transparency Specialist leads clinical trial transparency activities for assigned studies, helping ensure that trial registration and results information are ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Predicine, Inc

Clinical Trial Associate

Hayward, CA · On-site

$38.50 - $52.50/hr

Clinical Trial Associate Location: Onsite, Hayward, CA Department: Clinical Development Employment Type: Full Time Position Overview: The Clinical Trial Associate reports to Associate Director ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86K - $105K/yr

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable ...

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Clinical Trial Transparency Associate information

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How much do clinical trial transparency associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical trial transparency associate in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

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Senior Clinical Trial Transparency Specialist

Biogen

Remote

$116K - $155K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Biogen rating

9.3

Company rating: 9.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical

Job description

About This Role
The Senior Clinical Trial Transparency Specialist leads clinical trial transparency activities for assigned studies, helping ensure that trial registration and results information are disclosed accurately, on time, and in accordance with global requirements. You will serve as a key partner to study teams, internal stakeholders, and external vendors-coordinating planning, execution, quality oversight, and issue resolution across the disclosure lifecycle. This role contributes directly to Biogen's commitment to meaningful, patient-centered communication of clinical research information. You will also help strengthen the efficiency, quality, and consistency of Clinical Trial Transparency processes, technology, training, and vendor operations. This position reports to the Head, Clinical Trial Transparency Operations and works closely with Clinical Development, Regulatory Affairs, Medical Writing, Data Management, and external service providers.
What You'll Do
  • Lead disclosure planning and delivery for assigned clinical studies
  • Coordinate protocol registration, record maintenance, and results disclosure activities
  • Serve as the primary Clinical Trial Transparency contact for assigned study teams
  • Partner with vendors to deliver accurate, timely, high-quality registry disclosures
  • Monitor vendor workload, performance metrics, cycle times, and issue logs
  • Escalate disclosure risks, dependencies, and quality concerns as appropriate
  • Support planning, coordination, and quality review of plain language summaries
  • Improve Clinical Trial Transparency processes, work instructions, SOPs, and training
  • Provide user feedback and support testing for Clinical Trial Transparency technology solutions
  • Represent the function on cross-functional initiatives and continuous-improvement projects

Who You Are
You are a detail-oriented clinical research professional who is passionate about transparency, compliance, and making clinical trial information understandable and accessible to the public. You balance strong operational execution with a continuous-improvement mindset and enjoy collaborating across study teams, vendors, and internal functions. You are comfortable managing competing priorities, navigating complex global requirements, and translating them into clear, practical action.
Required Skills
  • Bachelor's degree in a science related field
  • 4+ years of relevant pharmaceutical-industry experience or equivalent
  • 2+ years experience of global clinical trial transparency knowledge and disclosure requirements
  • Experience with clinical trial registration and results disclosure activities
  • Understanding of clinical study and program communication-planning dependencies
  • Process mapping and continuous improvement experience
  • Vendor-management experience in an outsourced operating model
  • Ability to monitor deliverables, quality, timelines, metrics, and issues
  • Familiarity with Clinical Trial Transparency technology, systems, and tools
  • Knowledge of plain language summaries and patient-centered trial communication
  • Strong cross-functional communication and stakeholder-management skills

Preferred Skills
  • Experience supporting or leading SOP, work-instruction, or training updates
  • Familiarity with data sharing, patient engagement, health equity, or digital engagement

Job Level: Management
Additional Information
The base compensation range for this role is: $116,000.00-$155,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

Sourced by ZipRecruiter

At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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