Director, Clinical Scientist

Replimune•Woburn, MA

5d•Onsite

About The Position

Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response. The Director, Clinical Development/Clinical Scientist will report to the CMO or other senior member of the Clinical Development team to ensure the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. The Director, Clinical Development will be accountable to jointly develop clinical program strategy and work collaboratively with other functional representatives to assure that activities are executed within expected scope, compliance, budget, and timelines. The Director, Clinical Development will play a key role in the establishment and growth of Clinical Development functions to assure best-in-class global capabilities and execution. Specifically, the candidate will work closely with colleagues in clinical development, clinical operations, safety/pharmacovigilance, regulatory, biometrics, biomarkers and translational research, and program leadership.

Requirements

MD, PharmD, or PhD within a clinical and/or scientific profession (or an equivalent level of professional, clinical and/or scientific education, training and experience) required.
Minimum of 10 years of experience and success within other biotech/pharmaceutical companies.
Previous participation in a clinical development program is essential, including involvement in most stages of clinical trials (i.e. from start up to study report), ideally having taken at least one study through from start to finish in a clinical scientist or similar role.
Clinical oncology experience; candidates with exceptional experience in other therapeutic areas would be considered if they demonstrated clear potential to apply their existing skills to oncology.
Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing.
High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills
Knowledge of GCP and ICH Guidelines
Flexibility to work with colleagues in a global setting
Able to engage in work-related travel approximately 25%
Demonstrated success in working in a cross-functional environment
Experience with the development and support of related SOPs and policies is expected.
Knowledge of industry standard Clinical Development IT solutions expected.
Executive presence.
Values based collaborator – respectful, accountable and collaborative.
Ability to relate and work with a wide range of people to achieve results.
Impactful written and verbal scientific communication.

Responsibilities

Facilitate and execute the generation, author, update, and/or review of key clinical and regulatory documents, including, but not limited to: Protocol concepts, synopses, protocols, and amendments; Informed consent documents; Investigator Brochures; Clinical study reports; Abstracts, posters and manuscripts; Clinical sections of INDs (and equivalent applications), NDAs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports; Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports; Risks / benefits analysis for applicable documents; Clinical study supporting documentations and processes, e.g. charters for (independent) safety data monitoring or steering committee, study specific management plans and manuals, SOPs, etc.
Instrumental to the Clinical Development Plan Generation and Program Strategy
Primary contact and lead for all clinical and scientific aspects of the design, implementation, conduct, analysis, interpretation and documentation of clinical studies.
Partner with relevant functional areas for the successful implementation and execution of clinical studies.
Provide clinical and scientific expertise for selection of investigator and vendors
Train internal colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol
Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CROs
Review, query, and analyze clinical trial data
Serve as medical monitor or partner with (senior) medical director on medical monitoring, patient eligibility and study treatment related questions, in cooperation with the CRO or directly with study investigator
Interpret, and present clinical trial data, both internally and externally
Create clinical study or program-related slide decks for internal and external use
Represent a clinical study or development program on one or more teams or sub teams
Build and maintain opinion leader/investigator networks; organize and present at key opinion leader advisory boards and investigator meetings, engage advocacy groups
Contribute to or perform therapeutic area/indication research and competitor analysis
Build strong relationships with internal experts.
Identify continuous process improvement opportunities and help define/optimize standards and processes.
Identify incremental organizational resource needs – staff, budget, and systems.
Develop, track, execute and report on goals and objectives.
Support budget planning and management.
Be accountable for compliant business practices.