Clinical Trial Manager — Implantable Devices (Hybrid, Cambridge)

Biogen; Cambridge (MA); Hybrid; USD 117,000 - 157,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Stock purchase plan

Tuition reimbursement

Paid time off

Paid holidays

Parental leave

401(k) matching

Job summary

Biogen in Cambridge, MA is seeking a Clinical Trial Manager to support planning, coordination and execution of clinical studies within the Implantable Device Unit, ensuring trials run efficiently and compliantly.

You will work with cross-functional partners, study sites and external vendors to manage day-to-day trial operations, monitor progress, and drive data quality and participant safety under the Director of Device Clinical.

Qualifications

• Bachelor's degree and at least 5 years of experience in clinical research or clinical operations.
• Experience supporting studies of Class III implantable medical devices in a sponsor, CRO or clinical study site setting.
• Experience in vendor and site management.
• Strong organizational and communication skills.
• Ability to identify and resolve operational risks and issues.
• Knowledge of regulatory, safety, and quality protocols.

Responsibilities

• Support day-to-day clinical trial execution by tracking study activities and timelines.
• Collaborate with study sites, CROs, and external vendors to ensure trial conduct aligns with protocols and quality expectations.
• Monitor study progress and operational metrics, identifying and escalating risks or issues.
• Assist in vendor oversight and site management by reviewing performance and coordinating follow-up actions.
• Partner with internal stakeholders in Safety, Regulatory, and Quality to support consistent trial execution.
• Facilitate communication and action item follow-up with study sites and external vendors.
• Support the resolution of operational issues affecting study timelines or data quality.
• Prioritize study activities based on timelines, site needs, and agreed priorities.
• Coordinate routine communications and follow-up actions with study sites and vendors.
• Manage complex study execution issues involving multiple stakeholders and tight timelines.
• Organize and track study follow-up activities to ensure consistent execution across sites and vendors.
• Support management of vendor or site performance issues and coordinate communication to reduce impact on study execution.

Skills

Bachelor's degree

Clinical operations

Vendor management

Site management

Regulatory knowledge

Communication skills

Education

Bachelor's degree in a related field

Job description

Biogen in Cambridge, MA is seeking a Clinical Trial Manager to support planning, coordination and execution of clinical studies within the Implantable Device Unit, ensuring trials run efficiently and compliantly.

You will work with cross-functional partners, study sites and external vendors to manage day-to-day trial operations, monitor progress, and drive data quality and participant safety under the Director of Device Clinical.