Sr. Medical Director, Immunology, Clinical Development

Responsibilities

• Develop and implement the Clinical Development Plan for clinical pipeline and research assets.
• Lead and oversee the clinical development of early-stage assets through to registration and post-approval.
• Provide clinical insights for early development assets that have not completed R2D transition.
• Offer clinical input for assets in partnership with external partners and/or for in-licensing activities.
• Act as Research and Development Project Lead, ensuring accountability for an asset throughout development activities.
• Serve as a member of the functional leadership team, providing insights on broader strategy.
• Influence senior cross-functional counterparts across research, development, medical business, and commercial functions.
• Engage significantly with global regulatory authorities.
• Lead registration-stage programs and/or early clinical development programs with experience filing INDs.
• Participate in business development activities, including due diligence.
• Collaborate closely with MSIDU leadership, Immunology Franchise, and external innovation partners.

Requirements

• Required Skills:
• MD or MD, PhD, with training/experience in immunology, such as general medicine with a fellowship in rheumatology or dermatology, also considering pulmonary, ID, and GI.
• At least 5 years in the pharmaceutical industry.
• Experience leading registration-stage programs and/or early clinical development programs with experience filing INDs.
• Significant interaction with global regulatory authorities.
• Business development experience, including due diligence.
• Preferred Skills:
• Experience in rare indications is a plus.
• Ability to function as Research and Development Project Lead.
• Job Level: Management
• Additional Information
• The base compensation range for this role is: $278,000.00-$382,000.00
• 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

Benefits

Additional Information

About This Role: As the Sr. Medical Director specializing in Multiple Sclerosis and Immunology, you will be a pivotal member of our Clinical Development team. This role integrates scientific rationale, regulatory requirements, product development plans, and commercial goals to construct a strategic framework for our clinical development initiatives. You'll be responsible for developing and implementing the Clinical Development Plan (CDP) for both our clinical development pipeline and research assets. Leading and overseeing the clinical development of early clinical stage assets through to registration and post-approval is a core aspect of this position. You will provide critical clinical insights for early development assets, working alongside our research function. Your expertise will also be crucial in partnerships and in-licensing activities, where you will offer clinical input and participate in due diligence for potential external assets. This role not only demands deep clinical knowledge but also strategic acumen to influence broader organizational goals.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Biogen? Share your experience