Clinical Trial Manager, Class III Medical Devices

What You’ll Do:

• Manage day-to-day execution and coordination of clinical trials for Class III medical devices.
• Track study activities, timelines, deliverables, and operational issues in partnership with cross-functional team members.
• Coordinate with study sites, CROs, and external vendors supporting class III medical device trials to ensure protocol-required activities are performed according to timelines and quality expectations.
• Monitor study progress and operational metrics for class III medical device trials, identifying risks and issues that may affect timelines and data quality.
• Support vendor oversight and site management for class III medical device clinical trials by reviewing performance and operational quality concerns.
• Collaborate with internal stakeholders such as Safety, Regulatory, Quality, and Data Management teams.
• Assist with documentation, vendor oversight activities, and site management processes.
• Facilitate communication among internal team members, CROs, and sites to maintain study continuity.
• Support regulatory submissions, protocol amendments, and safety reporting workflows.
• Organize and track class III medical device clinical trial follow-up activities like action item logs and issue trackers.

Who You Are:

You are clinical trial professional with class III medical device expertise who thrives in a dynamic environment where attention to detail and organizational skills are paramount. You have a passion for ensuring the success and safety of class III medical device clinical trials, with the ability to navigate complex issues and coordinate multiple stakeholders effectively. Your proactive nature and excellent communication skills help you manage competing priorities and tight timelines with grace and efficiency. You are committed to fostering collaboration and maintaining high standards of quality and compliance in every aspect of trial management.

Required Skills:

• Bachelor’s degree; advanced degree preferred.
• At least 5 years of experience in clinical research or clinical operations.
• Experience supporting clinical trials for Class III implantable medical devices.
• Strong organizational and communication skills.
• Ability to track study progress and identify operational risks.
• Knowledge of regulatory and quality standards in clinical trials.

• Experience with vendor oversight and site management.
• Familiarity with regulatory submissions and protocol amendments.
• Expertise in safety reporting workflows and managing study changes.

Job Level: Management

Additional Information

The base compensation range for this role is: $117,000.00-$156,750.00

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.