Director of Translational Medicine

Found in: Resume Library US A2 - 2 weeks ago

Waltham Massachusetts, United States Deciphera Pharmaceuticals Full time
Job Description

We are seeking an experienced, highly-motivated and engaged Director of Translational Medicine.  The successful candidate will have extensive experience as a Translational Medicine lead for clinical trials ranging from Phase 1 through Phase 3.   This person will have an understanding of clinical development and experience developing clinically-relevant biomarkers.  The successful candidate will work closely with our Preclinical Research Team and our Clinical Development Team to develop clinical biomarker strategies for development candidates.  The Director will be a mentor and will build strong and supportive relationships with direct reports.  He/she will be an excellent communicator within the Translational Medicine Team as well as across functions.  He/she will be engaged and aligned with corporate and functional area goals and able to independently direct not only their own responsibilities but also those of their direct reports.

This position will be located in Waltham, MA and will report to the Executive Director, Translational Medicine located in the Waltham, MA office.

Key Responsibilities:

Reporting to Executive Director, Translational Medicine, this role will drive translational medicine strategy across multiple early-stage programs.

Develop and implement scientifically-driven yet practical clinical biomarker plan  to address key program-level questions in alignment with cross-functional team.

Direct or indirect involvement as Translational Medicine lead for multiple programs and studies.

Provide oversight of assay development and validation activities of multiple CROs from a technical, budget and timeline perspective.

Represent Translational Medicine on cross-functional teams and make strategic contributions to the clinical development plan.

Provide mentoring and support for direct reports.

Oversee biomarker data collection, analysis and interpretation for various presentations and publications.

Contribute to authoring/review of clinical study protocols, investigator brochures and additional documents as needed.

Responsible for budget and timeline across multiple studies/programs.

Establish effective communication with cross-functional colleagues including those from medical, clinical pharmacology, preclinical biology and biometrics.

Commitment to help the team achieve deliverables and meet aggressive timelines.

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