Senior Manager, Medical Coding

Senior Manager, Medical Coding

Who we are :

At Agios, we are fueled by connections to transform rare diseases. We foster an inclusive, collaborative culture – one that sparks bold thinking and strengthens our connections with each other and with the rare disease communities we serve. We embrace diverse backgrounds with respect, active listening, and a commitment to inclusion – because our differences shape how we hire, collaborate, and innovate. Our team’s proven track record of executional excellence, combined with our depth of expertise and dedication, enables us to develop innovative medicines that reflect the priorities of rare disease communities. Our commitment is more than scientific – it’s deeply personal, grounded in the meaningful connections we have built. To learn more, visit and follow Agios on LinkedIn and X.

The impact you will make :

Agios Pharmaceuticals is searching for a dynamic Senior Manager, Medical Coding to join our growing Clinical Data Management team. We want someone who cares about this important work, and who’s driven to connect to our mission of helping these patient communities. The Senior Manager, Medical Coding will be responsible for delivery of high-quality medical coding for individual clinical trials, clinical development programs, and regulatory submissions (Safety regulatory requirements as well as BLA submissions). He or she will be responsible for developing a long-term coding and dictionary strategy that will help to ensure that Agios meets industry and quality requirements for clinical trial, safety, and post marketing coding in a growing company. He or she will define and implement coding processes ensuring best practices in medical coding and dictionary management for both clinical trial and Safety coding. He or she will also serve as a subject matter expert for all topics pertaining to the use of medical coding data in statistical analysis, impact assessment, and safety signaling. This role is critical in ensuring integrity, accuracy and compliance of coded clinical trial data, ultimately contributing the success of clinical research initiatives and regulatory submissions.

What you will do :

• Responsible for all medical coding deliverables that support Agios’ regulatory commitments including submission of safety data and the preparation of the Integrated Summary of Safety (ISS) component of licensing applications. Identify opportunities for process optimization and efficiency enhancements in medical workflows.
• Maintain accurate documentation of coding processes, decisions. Preparing coding related reports, during reviews and dictionary upgrades. Develop and maintain coding and dictionary management processes for Agios in collaboration with key stakeholders. Review Program and study level clinical trial and safety coding performed by vendors for quality and consistency.
• Responsible for the development and ongoing evaluation of coding conventions to ensure consistency and optimize integration capabilities within and across therapeutic areas and Programs. Identify and mitigate potential risks as needed, implement strategies to address coding related challenges and minimize errors or discrepancies.
• Collaborate cross functionally as a SME for DM, Safety, and Biometrics and regulatory. Oversee routine and ad hoc impact analysis with pertinent MDs, particularly those related to bi-annual MedDRA dictionary up versioning; supports Safety in the development of expected lists for all clinical trial IMP and market products.
• Partner with Technical Systems and IT counterparts to optimize processes and technology that support efficient dictionary management and oversight of vendor quality.
• Develop and maintain strong relationships with external vendors performing clinical trial and safety coding, ensuring high quality deliverables, consistent application of coding conventions, implementation, and oversight of metrics to ensure quality and productivity, appropriate resourcing, and process improvements as necessary. Ensure that the vendor performance meets expectations and contractual requirements.

May oversee contractor and / or full-time staff.

What you bring :

Concerned that you don’t check off every box in the requirements listed above? Please apply anyway! At Agios, we value each other’s differences and recognize that teams thrive when everyone brings their unique experiences to the table. We are dedicated to building an inclusive, diverse, equitable, and accessible environment where all employees can bring their whole selves to work. If you’re excited about this role but your previous experience doesn’t align perfectly with the job description, we still encourage you to apply. You may be just the right candidate for this role or another opening!

Work Location :

Location Agnostic : Work location for this role is based on employee's individual preference. This role has the ability to be either remote in the US or hybrid in our Cambridge Headquarters. Hybrid schedules vary but are generally less than 3 days per week onsite and hybrid employees are expected to live within commutable distance to our Cambridge Headquarters. Remote employees work entirely from home except for attending Company sponsored events / meetings. For employees who choose to work remotely, travel may be required for certain company events commensurate to the above job description.

What we will give you :

Interested in learning more about what makes our culture unique? Visit the Inside Agios section of our website.