Senior R&D Project Manager — Drug Development (Hybrid)

TalentAlly; Boston (MA); Hybrid; USD 142,000 - 190,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life ins.

Fitness & Wellness reimbursement

Paid vacation & holidays

Sick time & Parental Leave

401(k) with company match

Employee stock purchase plan

Tuition reimbursement

Employee Resource Groups

Job summary

Biogen is seeking a Senior R&D Project Manager in Cambridge, MA to lead cross-functional project plans and ensure timely delivery of drug development milestones. You’ll partner with global teams to maintain integrated timelines, manage risks, and drive strategic initiatives.

Qualifications include a bachelor’s degree (advanced degree preferred) and 7+ years in pharma or PM, with experience in regulatory submissions and PM tools. Hybrid work with onsite weekly presence.

Qualifications

• Bachelor’s degree required; scientific focus preferred.
• Advanced degree (MS/MBA/PhD) preferred with relevant experience.
• Minimum 7 years in pharma, drug development, or PM.
• Experience with drug development processes and cross-functional PM tools.
• Regulatory submission planning experience desirable.
• Experience with integrated timeline development and PM systems.
• PMP certification a plus.

Responsibilities

• Ensure internal alignment and create integrated project timelines.
• Lead global Development plans and asset strategy alignment.
• Collaborate with cross-functional teams to deliver milestones.
• Manage workload, priorities, and agile execution.
• Foster teamwork across diverse teams and lead development efforts.

Skills

Project management

Cross-functional collaboration

Regulatory planning

Timeline/Gantt expertise

Effective communication

Decision making

Leadership

Education

Bachelor’s degree

Advanced degree preferred

Tools

Planisware

Microsoft Project

OnePager Pro/Express

MS Teams / Office 365 SharePoint

Job description

Biogen is seeking a Senior R&D Project Manager in Cambridge, MA to lead cross-functional project plans and ensure timely delivery of drug development milestones. You’ll partner with global teams to maintain integrated timelines, manage risks, and drive strategic initiatives.

Qualifications include a bachelor’s degree (advanced degree preferred) and 7+ years in pharma or PM, with experience in regulatory submissions and PM tools. Hybrid work with onsite weekly presence.