Director, Risk Evaluation & Mitigation Strategy (REMS) - Remote
Company: Agios Pharmaceuticals
Location: Schiller Park
Posted on: January 26, 2026
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Job Description:
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 www.agios.com and
follow Agios on LinkedIn and X. The impact you will make: Agios
Pharmaceuticals is searching for a dynamic Director, Risk
Evaluation & Mitigation Strategy (REMS) to join our growing Medical
Safety & Risk 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 Director, Risk Evaluation &
Mitigation Strategy (REMS) will be responsible for serving as the
organizational lead for the design, implementation, and oversight
of REMS programs. This role combines strategic leadership,
operational execution, and cross-functional collaboration. The
Director will reside within Medical Safety & Risk Management (MSRM)
and work closely with Regulatory Affairs, Medical Affairs, Market
Access, Commercial, Supply Chain, and Legal teams, as well as
external vendors, to deliver high-quality REMS programs that meet
FDA requirements and support product success. What you will do:
Strategic Leadership Lead the implementation, oversight, and
evaluation of REMS in alignment with the broader Program Strategy.
Act as the in-house REMS expert across the organization. Monitor
regulatory changes and proactively update strategies, policies, and
procedures to align with FDA requirements and best practices.
Partner with cross-functional teams to integrate REMS
considerations into product development, launch, and lifecycle
management strategies. Cross-Functional & Matrix Leadership
Responsible for the cross functional development of implementation
and operational plans that support the REMS. Accountable for REMS
management and oversight in accordance with time, cost and quality
commitments. Coordinate matrix teams across MSRM, Regulatory
Affairs, Medical Affairs, Market Access, Marketing, Quality, Supply
Chain, Commercial, and Legal. Communicate REMS strategy, progress,
and compliance metrics to senior management and governance
committees. Operational Execution Ensure timely execution of
operational aspects of REMS and related activities. Review REMS
related documentation, including FDA requests, and approve
vendor-authored documents as required. Oversee vendor interactions
and management of day-to-day REMS operations, ensuring compliant
enrollment, data collection, monitoring, and reporting. Support
integration of call centers, technology platforms, and other
operational infrastructure as appropriate. Approve and manage
program deliverables, budgets, and timelines. Develop and oversee
KPIs, dashboards, and compliance metrics to measure program
effectiveness. Ensure readiness for regulatory inspections and
audits; support noncompliance issue resolution, CAPA development
and execution as needed. What you bring: Qualifications Bachelor’s
or Advanced degree in science, pharmacy, nursing, healthcare, or
related field. 10 years of pharmaceutical/biotech industry
experience, with expert knowledge and proven track record on REMS
operations Proven track record in vendor management, program
implementation, and compliance oversight. Demonstrated success
leading cross-functional and matrix teams. Strong knowledge of FDA
REMS requirements and evolving regulatory landscape. Experience
implementing SOPs and compliance frameworks. Excellent
communication, project management, and organizational skills.
Preferred Advanced degree (PharmD, PhD, MSN, MPH, MBA, or related).
Audit and/or inspection experience in REMS and/or pharmacovigilance
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 employees 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:
Deliberate Development. Your professional growth as one of our top
priorities. Flexibility. We’re all about individual needs. We
embrace different perspectives, work styles, health and wellness
approaches, care of families and productivity. When you’re at your
best, we’re at our best. Premium benefits package. We invest in the
health, wellbeing, and security of our people with a premium
benefits package that is well-rounded and flexible to help meet the
varied personal and professional needs of every member of our team.
For more detail on the benefits we offer at Agios, visit the Inside
Agios section of our website. Competitive and equitable
performance-based compensation. This includes base salary and both
short- and long-term incentives that are connected to our business
strategy and vary based on individual and company performance. The
current base salary range for this position is expected to be
between $183,549 – $275,324 annualized; final salary will be
determined based on various factors including, but not limited to,
years of relevant experience, job knowledge, skills and
proficiency, degree/education, and internal comparators.
Psychological safety. We support an environment of fearlessness. We
want you to share your ideas, speak candidly and take data-informed
risks to help push the boundaries. Commitment to diversity. We
strive to foster a welcoming workplace where everyone can thrive.
We’re continuously looking to improve the inclusivity of our
workforce. Commitment to community. We’re an active participant in
the communities that surround us – the communities where we live,
and the community of people and their loved ones in need of better
treatment options for conditions that are often overlooked.
Keywords: Agios Pharmaceuticals, Joliet , Director, Risk Evaluation & Mitigation Strategy (REMS) - Remote, Science, Research & Development , Schiller Park, Illinois