Clinical Development Director Oncology
Location: Metro Washington DC Area
Clinical Development Director Oncology | Leading Global Biotechnology Company
This Clinical Development search is being conducted on behalf of our global biotechnology client. This is a unique opportunity to join our client at a time of tremendous growth and acceleration in the oncology biologics portfolio.
This is a fast-paced and dynamic work environment where, with increasing levels of responsibility, you will be responsible for medical monitoring of ongoing clinical trials, the planning and conduct of clinical trials and providing long-range clinical development planning.
One will also plan and manage clinical research projects and clinical development programs in oncology and collaborate with and provide clinical input and expertise to pre-clinical and translational sciences.
ADDITIONAL INFORMATION ABOUT THIS COMPANY AND ROLE:
Large Global Biotechnology Company with over 2,200 employees.
Dynamic environment that fosters collaboration and innovation.
This is a pivotal role in channeling the scientific capabilities to make a positive impact on changing patients’ lives.
A company is established, profitable, expanding and financially stable offering career growth.
Location: This company is located in the metro Washington DC area.
HIGHLIGHTS OF RESPONSIBILITIES:
Serve as medical monitor with primary responsibility for patient safety and conduct of assigned trials as well as overall data interpretation and safety surveillance.
Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports.
Responsible for assisting in design of clinical development plans and overall strategy for compounds, therapeutic classes of compounds or indications in light of developments in the area of clinical and pharmaceutical oncology.
Collaborate with pre-clinical and translational sciences, and senior management in assessing requirements for emerging products.
Provide leadership on cross-functional product development team(s) as experience allows.
Participate in identification, selection and conduct of negotiations with clinical research centers and investigators.
Participate in the selection and management activities of CROs.
Supervise project team members in planning, conducting and evaluating clinical trials.
Oversee planning and management of investigator meetings, advisory boards and other scientific committees.
DESIRED SKILLS AND QUALIFICATIONS:
MD degree, with current medical license and at least 2-5 years of experience in clinical research and/or oncology drug development in pharmaceutical or CRO environment.
Immuno-oncology development experience.
Experience in molecular oncology and/or translational science.
Medical specialty and sub-specialty training and certification (or eligibility in medical oncology or hematology for board certification).
To learn more about this role, contact a member of our team at firstname.lastname@example.org or 267-483-5233.
The Bandish Group, LLC
Life Sciences Executive Search
1432 Easton Road, Suite 2B
Warrington, PA 18976