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Job description
Overview
Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient’s lives depend on it.
At Replimune, we live by our values:
United: We Collaborate for a Common Goal.
Audacious: We Are Bold.
Dedicated: We Give Our Full Commitment.
Candid: We Are Honest With Each Other.
People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.
Join us, as we reshape the future.
Summary of job description:
This function will serve as a field based medical expert and will be responsible for building/strengthening collaborative relationships in support of Replimune clinical development initiatives. This will be fulfilled mainly through the development of excellent working relationships with key opinion leaders, clinical sites, and internal stakeholders. Additional responsibilities include collection and internal dissemination of competitive intelligence, supporting portfolio expansion, and driving key pre-launch, launch, and post-marketing initiatives.
This is a field-based position.
Key responsibilities:
Identify key national and regional oncology thought leaders and priority customers, build and maintain advocacy with these individuals, and function as their primary scientific contact with Replimune.
Participate in the collection and exchange of scientific/technical information important to Replimune development efforts (serve as a field-based extension of the in-house clinical team).
Assist in the management of relationships between key opinion leaders and corporate product teams.
Accumulate key competitive information to aid the clinical and marketing teams in product/brand development.
Identify, initiate, coordinate, evaluate and monitor investigator-sponsored studies intended to support the clinical and scientific strategy of Replimune products.
Help develop and manage to timelines publication plans of investigator-sponsored studies.
Assist in the identification, evaluation and engagement of potential investigators for Replimune corporate trials.
Assist the clinical trials team, as needed, in the ongoing support and communication with investigators on Replimune corporate trials.
Education of priority customers on research and development projects.
Develop key advocates as speakers to support Replimune products and strategies.
Assist in the development of, and participate in, regional advisory boards and medical education programs
Contribute scientific and clinical expertise to the development and execution of commercial educational activities.
Provide clinical resources for programs supporting sales/sales training and marketing efforts and professional services.
Represent Replimune at major oncology meetings and conferences, including regional meetings as needed.
Maintain clinical and technical expertise in the area of oncology through review of the scientific literature and attendance at key scientific meetings.
Serves as role model to team members:
Takes initiative and perform tasks in a self-directed manner
Demonstrates professional behavior when interacting with Health Care Professionals and internal colleagues
Demonstrates positive attitude toward company and colleagues
Enhances cohesiveness among MSL team members – providing a respectful, inclusive environment
Proactively offers ideas and solutions to enhance the productivity of the Medical Science Liaison Team
o Adheres to the Replimune Code of Business Conduct & Ethics
Leads assigned projects within the MSL organization
Spearheads strategic initiatives within the MSL organization in collaboration with Directors
Delivers updates and presentations to Medical Affairs senior management
Develops best practices for the MSL team
Delivers scientific / clinical presentations at advisory boards, consultant meeting, and/or facilitation of breakout sessions
Delivers scientific / clinical presentations to payor groups and other managed market customers
Represents MSL team on select clinical / medical study teams
Other responsibilities
Educational requirements:
Advanced degree in medical science (MD, PharmD, or PhD) is strongly preferred. Candidates without an advanced degree are required to have at least 1 year of industry MSL experience in the therapeutic area, and 2-5 years overall related experience.
Candidates with a Nurse Practitioner level degree or equivalent and 5+ years of clinical or industry experience in oncology may also be considered.
Experience and skill requirement:
At least 1 year of previous MSL experience in the therapeutic area of interest required
Candidates with a Nurse Practitioner level degree or equivalent and 5+ years of clinical or industry experience in oncology may also be considered.
Patient care clinical experience in the therapeutic area (including sub-specialty) preferred
Leadership experience (with direct reports or as an individual contributor) is a preferable trait
Strong project leadership and management history required.
Ability to efficiently manage time and priorities.
Strong leadership skills and the ability to compile and disseminate information to others in a cohesive fashion to assure a clear understanding of project status and direction.
Solid understanding of drug development and life-cycle development of a product.
Ability to cultivate and maintain relationships with thought leaders and to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through to requests from thought-leaders; the ability to work effectively with key decision makers, both within and outside the Company.
Excellent communicator, skilled at diplomacy and capable of effectively combining science and relationship building.
Ability to understand and translate external customer and/or internal client needs into effective decisions and to drive results and strive for continuous improvement with high performance in the face of adversity a must.
Willingness to travel extensively.
Salary Range
Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $208,500-$269,500. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate’s unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.
At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.
About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune’s proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit
We are an Equal Opportunity Employer.
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Worksite address
woburn, MA, 01813, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.