Reporting into the VP, Early Clinical Development (VPCD), the  Medical Director, Clinical Development will be assisting in the implementation of the Replimune drug development strategy and will be taking a leadership and contributor role in enabling all aspects of individual drug programs. They will lead or support conduct of clinical studies and will work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research. The Medical Director will provide clinical input on clinical protocol development, regulatory interactions, patient enrollment to clinical studies, safety monitoring and review, biomarker development, implementation and analysis of data, manuscript writing and submission, and presentation of data at national and international meetings. The  Medical Director will have both an inward and outward facing presence, including assisting the clinical operations team in the site evaluation and selection process for assigned clinical trials. This position may also work closely with preclinical functions and may be involved in interactions with strategic or collaboration partners.

There is a strong preference for a local candidate who can be on site in our Woburn, Massachusetts headquarters a minimum of 2 days per week 

Key responsibilities:

• Contributes to the overall clinical strategy for all or select RP programs from early development, through regulatory submissions and post-commercialization, with an emphasis from mid to late stages of
• Serve as Replimune’s clinical lead and point person on assigned programs and clinical trials from initiation to study discontinuation. Leads or facilitates cross-functional clinical development and/or study team(s) on the following activities, including but not limited to:
  • Designs studies as per clinical strategy, driving clinical activities related to preparation and approval of synopses, protocols and the conduct of clinical studies.
  • Responsible for the relevance and accuracy of medical science underpinning of clinical study based on thorough scientific review and consultation with internal and external
  • Organizes and conducts consultations with global opinion leaders and

contributing to or even leading Advisory Board meetings.

• Reviews and finalizes the medical and scientific portions of clinical study concepts and clinical study protocols and
• Reviews and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory
• Responsible for oversight of cross-functional study team and provides medical guidance to the clinical study

• Responsible for medical monitoring activities in partnership with CRO, pharmacovigilance, biostatistics, clinical operations, and program leadership for, including but not limited to,
  • Assessing issues related to study conduct
  • Individual subject safety, in partnership with CRO responsible for trial
  • Program, trial or data risks, creating, and implementing mitigation strategies
  • Maintains and develops relationship with key study investigators
• Provide medical input and guidance to development and study/project teams and work collaboratively with cross-functional team members, such Data Management, Medical Directors and Clinical Scientists, Medical Safety and Pharmacovigilance and Medical Affairs to coordinate real time availability of clinical trial data, assuring data integrity, including safety, efficacy, pharmacokinetic, and correlative studies data to provide consolidated information for trial progress. Direct the interpretation of clinical and translational study data. Presents to internal governance committee or management and helps determine how individual study results impact the overall compound
• Authors/contributes to clinical sections of communications/documentation for regulatory agencies and is a key contributor in meetings with agencies. Supports generation and coordination of clinical documents and deliverables in support of regulatory filings, such as clinical study reports, DSURs, PSURs, regulatory submission sections, and investigator’s brochures, as well as provides input to regulatory
• Ensures that all the activities and clinical programs are in compliance with the GCP and regulatory requirements, as well as local and institutional
• Work with the Regulatory team and other cross functional representatives to ensure the timely preparation of high-quality documents to be submitted to the FDA and other health authorities for review, and represent Clinical at meetings with the FDA, EMEA and other regulatory
• Work with program management to assure deep integration of objectives, achievement of milestones according to the timelines, and optimal use of resources across
• Support the tactical development of clinical trials programs, including the prioritization of investigator sponsored studies in the context of the overall clinical strategy, and literature reviews.
• Collaborate with Medical Affairs on the development of educational materials intended for all stakeholders, including healthcare providers and patients, that is medically accurate and
• Maintain understanding of competitors and clinical developments in relevant therapeutic areas by attending scientific meetings and tracking
• Ensure the consistent application of state-of-the-art scientific and ethical methods to design clinical investigational trials of the highest
• Help assure that all activities within clinical development are executed compliantly and to global industry standards as well as within expected scope, budget and
• Collaborate with colleagues in research and preclinical development functions to move product candidates from entry into clinical
• Actively support business development to evaluate product candidates, determine product indications and assist in related strategic planning and partnering

Other responsibilities:

• Completes and maintains Compliance training; provides input on new initiatives and makes recommendations on new compliance procedures; assists in the development of compliance and quality training

• Will work with commercial to develop a commercialization strategy which will include development of TPPs based on competitive assessment and target positioning and will align the clinical development strategy with the commercial strategy, and may include the design of post-marketing studies, as
• May be asked to serve on Replimune internal committees, as
• May be asked to serve as a Replimune representative on external committees and foundations, as
  • Assists with the recruitment of new employees, mentors junior team members, contributes to relevant training materials, as well as provides guidance and assistance in new hires’ professional
• Other duties as required 

Educational requirements:

• A medical degree (M.D.) is required, additional science degree (PhD) desirable but not required. Training and experience in oncology and immunotherapy is required.
• Oncology board certification strongly preferred

Experience and skill requirements:

• Minimum 5 years of global clinical development experience and success within other biotech / pharmaceutical
• Professional knowledge and skills working with solid tumor oncology
• Must possess a high level of understanding of the fundamentals of clinical development, such as experience with protocol development and follow up, including but not limited to: Study monitoring, data collection and analysis, database cleaning and database
• Demonstrated experience in designing development strategies (including role of biomarkers) and leading Phase 1-3 programs coupled with the appropriate regulatory and commercial experiences of successful oncology drug product approval and
• Proactive, creative, forward-thinker with the ability to think innovatively about integrated strategy for research, clinical and commercial activities, while accurately anticipating future consequences and
  • Knowledge of all the requirements and processes needed to take a drug candidate through clinical development to registration
  • Experience in late stage medical affairs and commercial environments, including the planning of and participation in pre-commercial activities for late stage to commercial products
• Demonstrated familiarity with biostatistics principles used in the analysis and interpretation of clinical trial
• Familiarity with and ability to interface effectively with appropriate Key Opinion Leaders (KOLs), investigators, CROs, and other
• Excellent written and verbal scientific communication skills and analytical
• Knowledge of applicable International Compliance guidelines and regulations, FDA, EMA, PMDA regulations and expectations, Good Clinical Practice, ICH guidelines, and clinical drug
• Experience in representing the sponsor in front of regulatory
• Knowledge of the day-to-day medical monitoring of clinical trials (e.g., responding to questions about patient eligibility and protocol waivers; review of safety parameters; working closely with Pharmacovigilance on processing SAEs, including the composition of SAE narratives; and IND expedited safety reports).
• Prior experience with vendor selection and management is
• Experience with the development and support of related SOPs and policies is
• Experience with partnerships and strategic alliances is
• Skilled in multiple computer-based tools, in addition to software programs such as Word, Project, PowerPoint, Excel,
• Domestic and international travel (up to approximately 30%) is required
• strong preference for a local candidate who will be on-site in our Woburn Headquarters 2-3 days per week