Sr. R&D Project Manager

Posted 16 Days Ago
Be an Early Applicant
2 Locations
In-Office or Remote
142K-190K Annually
Senior level
Biotech
The Role
Leads cross-functional pharmaceutical development projects and strategic R&D initiatives. Responsibilities include creating integrated development plans and timelines, managing scope, tracking milestones and deliverables, mitigating risks, coordinating global teams, ensuring functional alignment, and communicating project status. The role supports drug development programs and regulatory submission planning while driving disciplined, collaborative execution across the development portfolio.
Summary Generated by Built In

This role is based in Cambridge, MA and follows a hybrid work arrangement with weekly onsite presence. However, remote work may be available for highly qualified candidates residing within the United States.


Job Description 

Are you excited by an opportunity to leverage your project management expertise? Bring your skills and talents to Biogen and our Development Project Management Team, where you’ll have the opportunity to make an impact on the lives of patients around the globe.  The Program and Portfolio Management (PPM) department provides strategic and operational drug development leadership across the Development portfolio, integrating drug development across all functions and translating strategy into execution to deliver medicines to patients. 

As the Senior R&D Project Manager, you will partner with your Development Asset Leads and work collaboratively with your global cross-functional project teams to progress the Biogen Development portfolio.  You will ensure high-quality project planning and execution of drug development programs as well as strategic R&D initiatives. You are responsible for ensuring internal functional alignment, creating integrated project timelines, tracking, and verifying completion of project deliverables and milestones, identifying and mitigating project risks, and timely communication to relevant partners via regular and ad-hoc status reports.   

 

What You’ll Do 

  • Ensure internal functional alignment, creating integrated project timelines, tracking, and verifying completion of project deliverables and milestones, identifying and mitigating project risks, and timely communication to relevant partners via regular and ad-hoc status reports. 
  • Manage scope and support creation of a global Integrated Development Plan that articulates the asset strategy and provides foundation for operational objectives 
  • Collaborate with Development Project Teams to create and execute project plans and delivery of project milestones 
  • Proficient in self-management and organizational skills; able to manage workload, set personal and team priorities and adjust as needed  
  • Strong interpersonal and teambuilding skills; able to develop effective teamwork between team members with diverse styles  
  • Lead Development teams with judgment-based decisions 

Who You Are: 

You work collaboratively with your global cross-functional project teams to progress the Development portfolio.  You ensure high-quality project planning and execution of drug development programs. 


Qualifications 

  • Bachelor’s Degree required – scientific focused degree is a plus
  • Higher degrees (e.g. MS, MBA, PhD) preferred, ideally with a scientific focus 
  • Minimum 7 years of experience in the pharmaceutical industry, drug development, or project management. An advanced degree in a relevant discipline may be considered in combination with relevant industry experience.
  • Knowledge of, or previous experience with, drug development processes and application of project management tools and processes in cross-functional settings  
  • Proficient experience in Global Regulatory submission planning for drug development (IND submissions, Regulatory filing requirements, schedules, and dependencies across relevant functional areas) is desirable 
  • Proficiency with integrated timeline/Gantt chart development and technical experience with project management systems & collaboration tools is a plus (e.g. Planisware, Microsoft Project, OnePager Pro/Express, MS Teams, O365 SharePoint 
  • Outstanding ability to communicate effectively both verbally and in writing; ability to communicate to a broad range of stakeholders 
  • Ability to work independently, navigate ambiguity, adapt to change and make rapid, disciplined decisions to enable agile execution 
  • Proven ability to network and collaborate across multiple teams with agility and ability to get results 
  • PMP certification is a plus 

Salary base varies depending on location.


 

Job Level: Management


Additional Information

The base compensation range for this role is: $142,000.00-$190,000.00


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. 


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.



Skills Required

  • Bachelor's degree required; a scientific-focused degree is preferred
  • Minimum 7 years of experience in the pharmaceutical industry, drug development, or project management
  • Knowledge of drug development processes and project management tools and processes in cross-functional settings
  • Strong verbal and written communication skills with the ability to communicate with diverse stakeholders
  • Ability to work independently, navigate ambiguity, adapt to change, and make disciplined decisions
  • Ability to network and collaborate across multiple teams and deliver results
  • Higher degree such as MS, MBA, or PhD, ideally with a scientific focus
  • Experience with global regulatory submission planning, including IND submissions, filing requirements, schedules, and dependencies
  • Experience developing integrated timelines and Gantt charts
  • Experience with project management systems and collaboration tools such as Planisware, Microsoft Project, OnePager, Microsoft Teams, or SharePoint
  • PMP certification

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation — Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility — Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth — Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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