Senior Director, Medical Affairs

Job Description

Job Description

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.  Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.   

Why Choose Editas? 

At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor! 

Decoding The Role: 

The primary focus of this role is to lead medical and scientific strategic planning and operational execution of core medical affairs activities from early-clinical phase through lifecycle management for our lead in vivo development candidate, EDIT-401, a potential best-in-class, one-time therapy designed to significantly reduce LDL cholesterol levels. This role will build Medical Affairs capabilities while providing scientific leadership and strategic direction across cross-functional teams and strong engagement with external stakeholders. 

As the Senior Director, Medical Affairs you will: 

• Develop and lead Medical Affairs strategies including medical communications, engagement with opinion leaders, data dissemination, and external collaborations 

• Establish and execute a strategic publication and congress plan; work with internal colleagues to develop key messages on unmet need, mechanism of action, and target product profile 

• Build core scientific platforms, disease-state education materials, and standard medical response documents working closely with Clinical Development, Regulatory, Research, and Legal to develop a consistent, compliant scientific narrative 

• Serve as internal medical-scientific expert, providing scientific interpretation of data (clinical trials, real-world evidence, published literature) and translating insights into actionable medical strategy 

• Cultivate and maintain trusted relationships with the medical community by driving scientific exchange with thought leaders, investigators, steering committees, and medical societies. 

• Design and lead scientific advisory boards to gather insights on clinical trial designs, patient selection criteria, target product profile and lifecycle planning 

• Partner with Clinical Operations and Clinical Development to provide input in design and execution of clinical trial programs and facilitate enrollment of company sponsored clinical trials 

• Engage with patient advocacy organizations to build trust and awareness within the community 

• Direct external medical communication agencies, manage operational budgets, and mentor internal team members 

Requirements

The Ideal Transcript: 

To thrive in this role, you’ll need: 

• Advanced health/life sciences degree (PhD, PharmD, or MD)  

• 10+ years in biopharma Medical Affairs or Scientific Communications, experience with one-time curative intent therapies and early clinical phase development preferred 

• Successful record of achieving and maintaining compliance with all applicable regulatory, legal, and operational rules 

• Demonstrated experience building productive relationships with internal stakeholders and external stakeholders including KOLs and patient advocacy groups 

• Excellent written and oral communication skills with the ability to influence senior leadership, cross-functional partners, and external stakeholders. 

• Capacity to critically analyze and interpret complex scientific data and translate it into medical strategy 

• Track record of planning, initiating, and completing high-impact projects within established timelines. 

• History of thriving in ambiguity, managing multiple priorities while maintaining focus on achieving defined objectives 

Benefits

Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy. 

Salary Range:

$280,000 - $325,000 

Pay Transparency  

Editas Medicine is committed to transparency and accuracy in our hiring practices. The anticipated salary range for each position is posted within the role. The final salary offer will be determined based on a comprehensive assessment of the candidate's qualifications, including education, training, and relevant experience. Additional factors such as external market conditions, the role's criticality, and internal equity will also be considered. Editas Medicine's compensation philosophy ensures fair and equitable pay practices. 

Aspire to be an Editor?We invite you to apply and join us at the forefront of innovation and be a key contributor to realizing Editas Medicine's mission of developing transformative medicines for people living with serious diseases.