Biogen
Director, Development Asset Lead
Cambridge, MA · Director · Full-time
Sponsorship not specified$217k-$299kDetected 28 days ago
Project ManagementExcelAnimal StudiesLeadershipCommunicationCollaboration
About the role
- Your role is integral in providing strategic, multi-disciplinary drug development expertise to maximize asset value and delivery.
- This position requires seamless collaboration across functions, ensuring all voices are heard and integrating business considerations of time, risk, and value into planning and execution.
- You will be accountable to governance mechanisms for asset-related actions and decisions, representing the asset at portfolio forums and engaging with senior stakeholders.
Responsibilities
- Lead the development and ongoing refinement of the integrated plan for one or more assets to maximize value creation and execution.
- Establish and maintain clear asset goals, timelines, and risk management in partnership with project management functions.
- Drive accountability of functional team members and delivery of functional-level plans that integrate with overarching asset strategies.
- Engage proactively with stakeholders and governance to support asset execution and portfolio decision-making.
- Create and maintain conditions for a strong team culture that facilitates effective planning and execution of the asset strategy.
Requirements
- You are a strategic thinker with a robust understanding of drug development processes.
- Required Skills:
Nice to have
- Advanced degree strongly preferred (MS/MD/PhD/PharmD/MBA).
- Bachelor's degree required
- Preferred Skills:
Skills
- Bachelor's degree required; Advanced degree strongly preferred (MS/MD/PhD/PharmD/MBA).
- 10+ years of drug development experience in pharma or biotech.
- Demonstrated track record of strategic leadership in cross-functional teams.
- Experience in creating and executing clinical development plans aligned with strategic goals.
- Understanding of competitive and business implications of scientific and medical data.
- Experience in global regulatory requirements and processes for drug development.
- Knowledge of regional or country-specific requirements for patient populations and clinical endpoints.
- Proven ability to integrate commercial and competitive considerations into development strategies.
- Job Level: Management
- Additional Information
- The base compensation range for this role is: $217,000.00-$299,000.00
Compensation
- Tuition reimbursement of up to $10,000 per calendar year
Benefits
- Medical, Dental, Vision, & Life insurances
- Fitness & Wellness programs including a fitness reimbursement
- Paid Maternity and Parental Leave benefit
- 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)
- Employee stock purchase plan
- 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.
Company info
- Up to 12 company paid holidays + 3 paid days off for Personal Significance
- 401(k) program participation with company matched contributions
- 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.
This listing is sourced directly from Biogen's careers page and normalized into a canonical job model.