The Director Clinical Research, Oncology is a member of a matrix team dedicated to the implementation of clinical research studies that are part of a global compound development program. The Director supports the Medical Leader/Clinical Leader and provides active scientific contributions to a cross-functional clinical team developing a compound currently being studied for new oncology applications. Other functional groups represented on the team include project management, regulatory affairs, global clinical operations, data management, medical writing, biostatistics, medical affairs, clinical pharmacology, and health economics.
High-performing and energetic individual who demonstrates outstanding scientific knowledge applicable to oncology clinical research and the highest personal and ethical standards.
The successful candidate must be equally comfortable among the team to which he/she is assigned and in the global environment in which the company operates.
The Director of Clinical Research, Oncology, will be the key physician contact for sites and investigators during site start-up and study execution.
The Director will act as a liaison between the company and clinical investigators.
He/She will develop, in concert with senior clinical staff, credible relationships with opinion leaders.
He/She will be providing leadership for Phase 3 studies.
He/She will be participating in the data cleaning, medical review ,interpretation and reporting of the results of the research, including submission to health authorities.
He/She evaluates scientific information and new ideas to assist in identifying new research opportunities.
The Director supports medical affairs activities involving product evaluation, labeling and surveillance.
The Director Clinical Research, Oncology reports directly to a Medical Leader/Clinical Leader for the product to which he/she is assigned.
Qualifications
Qualifications:
This position requires a minimum of an advanced degree in medicine (i.e. M.D or DO or equivalent).
A trained Oncologist (Board certified or Board Eligible or equivalent) is strongly preferred.
Applicable post-doctoral fellowship training is required.
A minimum of 3 or more years of experience in a clinical research position, in oncology, within the pharmaceutical industry is preferred.
Significant knowledge of basic and clinical cancer research and its application to cancer drug development is important.
A strong commitment to oncology/hematology clinical research and the ability to work well within a team setting are essential
Good oral, written communication and presentation skills (including report development) are essential.
Successful work experience in a matrix team environment with cross functional teams is required.
Travel required may be up to 20 % annually (international, as well as domestic).
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