Clinical Trial Data Transparency Jobs (NOW HIRING)

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.

• 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.

• 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

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

Management

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.

• 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

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.