Sr. R&D Project Manger

Biogen; Cambridge (MA); Híbrido; USD 142 000 - 190 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Medical, Dental, Vision, & Life ins

Fitness reimbursement

Vacation and holidays

401(k) match

Employee stock purchase plan

Tuition reimbursement

Resumo da oferta

Biogen in Cambridge, MA is seeking a Senior R&D Project Manager to lead cross-functional drug development programs within the Development Project Management Team. The role collaborates with asset leads worldwide to ensure high-quality planning, execution, and timely deliverables across the portfolio.

The position is based in Cambridge with a hybrid schedule, including regular onsite presence. A Bachelor's degree is required, and 7+ years in pharma or project management are expected; advanced

Qualificações

• Bachelor’s Degree required; advanced degrees preferred.
• 7+ years in pharmaceutical industry, drug development, or project management.
• Knowledge of drug development processes and PM tools.
• Experience with regulatory submission planning (INDs) is desirable.
• PMP certification is a plus.

Responsabilidades

• Develop integrated project plans and timelines.
• Collaborate with global cross-functional teams.
• Identify and mitigate risks; track milestones.
• Provide timely status updates to stakeholders.
• Lead teams with sound, disciplined decisions.

Conhecimentos

Project management

Cross-functional

Communication

Leadership

Teamwork

Formação académica

Bachelor's degree

Advanced degree preferred

Ferramentas

Planisware

Microsoft Project

OnePager Pro/Express

MS Teams

SharePoint

Descrição da oferta de emprego

This role is based in Cambridge, MA and follows a hybrid work arrangement with weekly onsite presence.Job DescriptionAre 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 DoEnsure 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 objectivesCollaborate with Development Project Teams to create and execute project plans and delivery of project milestonesProficient in self-management and organizational skills; able to manage workload, set personal and team priorities and adjust as neededStrong interpersonal and teambuilding skills; able to develop effective teamwork between team members with diverse stylesLead Development teams with judgment-based decisionsWho 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.QualificationsBachelor’s Degree required – scientific focused degree is a plusHigher degrees (e.g. MS, MBA, PhD) preferred, ideally with a scientific focusMinimum 7 years of experience in the pharmaceutical industry, drug development, or project management. A n 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 settingsProficient experience in Global Regulatory submission planning for drug development (IND submissions, Regulatory filing requirements, schedules, and dependencies across relevant functional areas) is desirableProficiency 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 SharePointOutstanding ability to communicate effectively both verbally and in writing; ability to communicate to a broad range of stakeholdersAbility to work independently, navigate ambiguity, adapt to change and make rapid, disciplined decisions to enable agile executionProven ability to network and collaborate across multiple teams with agility and ability to get resultsPMP certification is a plusJob Level: ManagementAdditional InformationThe base compensation range for this role is: $142,000.00-$190,000.00Base 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 insurancesFitness & Wellness programs including a fitness reimbursementShort- and Long-Term Disability insuranceA 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 Significance80 hours of sick time per calendar yearPaid Maternity and Parental Leave benefit401(k) program participation with company matched contributionsEmployee stock purchase planTuition reimbursement of up to $10,000 per calendar yearEmployee Resource Groups participationWhy 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.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.