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Cumberland FarmsSOUTH DARTMOUTH, MA, USSenior Director / Vice President, Program Leader
Run my Accounts AGMA, United States- Full-time
Location
Greater Boston area
Role Description
The Senior Director / Vice President, Program Leader will be responsible for overseeing the strategy, execution, and the progression of the Company’s drug development programs from preclinical through clinical development, regulatory approval, and product launch. This role requires leadership of cross-functional teams, collaboration with internal and external stakeholders, and ensuring alignment with corporate objectives and timelines. The ideal candidate will possess deep scientific knowledge, strong strategic vision, and demonstrated experience managing complex drug development programs.
Responsibilities
- Program Management :
Drive Program Strategy and Execution :
Lead cross-functional teams across various functions (e.g., medical, bioanalytical, clinical operations, regulatory affairs, CMC, and marketing) to ensure effective progression of the drug development program; will also collaborate closely with Project Managers, as needed.
Accountable for development and management of program budgets.
Communicate clearly with external partners, if applicable, to ensure programs goals and timelines are understood and progress is tracked by both parties.
Integrate Scientific and Strategic Direction :
Lead the integration of preclinical, clinical, and regulatory strategies, ensuring scientific discoveries are translated into clinical advancements.
Collaborate with clinical teams on protocol design and execution to align with program strategy and regulatory requirements.
Ensure that all program activities are compliant with applicable regulations and ethical standards.
Cross-functional Team Leadership :
Build and lead cross-functional core project teams, including medical, bioanalytical, clinical operations, regulatory affairs, CMC, and marketing.
Identify and Mitigate Program Risks :
Ensure identification of risks in scientific, operational, and regulatory domains and implement mitigation strategies.
Utilize data-driven insights to make informed decisions and adjust the program strategy when necessary.
Market and Competitive Analysis :
Collaborate with marketing resources to assess market needs, competitive positioning, and ensure the drug development program aligns with commercial objectives.
Provide expertise / input as needed during partnering discussions, review of partnering documents and filing of IP related to the program.
Requirements
Knowledge & Skills
Compensation and Benefits
Competitive base salary, eligibility for an annual incentive bonus and eligibility to participate in company stock option plan. Competitive benefits package including health, dental, vision, life insurance, 401K and paid time off.
About Acumen Pharmaceuticals
Acumen, headquartered in Newton, MA, with offices in Indianapolis, IN and Charlottesville, VA, is a clinical-stage biopharmaceutical company developing a novel therapeutic that targets toxic soluble amyloid beta oligomers (AβOs) for the treatment of Alzheimer’s disease (AD). Acumen’s scientific founders pioneered research on AβOs, which a growing body of evidence indicates are early and persistent triggers of Alzheimer’s disease pathology. Acumen is currently focused on advancing its investigational product candidate, sabirnetug (ACU193), a humanized monoclonal antibody that selectively targets toxic soluble AβOs. Acumen is currently conducting the ALTITUDE-AD study, a Phase 2, multi-center, randomized, double-blind, placebo-controlled clinical trial currently enrolling at sites in the United States and Canada, with plans for additional study centers in Europe and the UK, following positive results in INTERCEPT-AD, a Phase 1 clinical trial involving early Alzheimer’s disease patients.
Equal Employment Opportunity
Acumen Pharmaceuticals provides equal employment opportunities to all employees and applicants without regard to race, color, religious creed, sex, national origin, ancestry, citizenship status, pregnancy, childbirth, (or related medical conditions, including, but not limited to lactation), physical disability, mental and / or intellectual disability, age, military status or status as a Vietnam-era or special disabled veteran, marital status, registered domestic partner or civil union status, gender (including sex stereotyping and gender identity or expression), medical condition (including, but not limited to, cancer related or HIV / AIDS related), genetic information, sexual orientation or any other characteristic protected by applicable federal, state and local law.
Accommodation Of Disabilities
Acumen Pharmaceuticals is committed to providing reasonable accommodation for qualified applicants and employees with a disability (including veterans with a disability), unless such accommodation would cause an undue hardship.
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