[Hiring] Clinical Trial Manager @Biogen

Role Description

As a Clinical Trial Manager, you will be integral to the planning, coordination, and execution of clinical trials for Class III medical devices, ensuring they are conducted in compliance with regulatory and quality standards. You will be part of the Implantable Device Unit team, working closely with cross-functional partners, study sites, and external vendors to support effective trial operations. Your role is crucial for tracking study progress, identifying operational risks, and contributing to the resolution of issues affecting timelines and data quality. You will support trial documentation, vendor oversight, and site management processes, playing a key role in delivering successful clinical trials under the leadership of the Director, Device Clinical. This position offers an opportunity to impact the overall business by ensuring the safety and efficacy of class III medical devices that enhance patient care.

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.

Qualifications

• 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.

Benefits

• 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