(Sr) Medical Director

2 weeks ago


New York State, United States Avetix Group Full time
About the positionWe are looking for a (Senior) Medical Director, Oncology TA Head to lead and oversee the medical strategy for the oncology therapeutic area. You will play a crucial role in the development and implementation of clinical programs and provide medical expertise to support the overall therapeutic area strategy.

First-in-human Phase 1 and Phase 2 experience is a mustEssential Job Functions:Medical Strategy: Develop and execute the medical strategy for the oncology therapeutic area, in alignment with the overall company goals and objectives. This includes identifying key medical insights, unmet needs, and opportunities for clinical development.Clinical Development: Provide medical leadership and guidance in the planning, design, and execution of clinical trials. Collaborate with cross-functional teams to ensure the successful implementation of clinical programs.Medical Expertise: Serve as a subject matter expert in oncology, staying up-to-date with the latest scientific and medical advancements in the field. Provide medical support and insights to internal stakeholders, including preclinical teams, regulatory affairs, and clinical operations and also external stakeholders, including supporting business development meetings.KOL Engagement: Foster relationships with key opinion leaders (KOLs) in the oncology field. Engage in scientific exchange and collaborate on research initiatives to advance the understanding and treatment of oncology diseases.Team Leadership: Provide leadership and mentorship to a team of medical professionals within the oncology therapeutic area. Foster a collaborative and high-performing team culture, encouraging professional growth and development.

Qualifications:Medical Doctor (MD) degree is required and MD degree with specialization in oncology is a plus.Proven experience in

early clinical development in oncology

area within the pharmaceutical industry.Excellent understanding of clinical trial design, execution, and regulatory requirements.Demonstrated leadership skills with the ability to influence and collaborate across cross-functional teams.Exceptional communication and presentation skills, with the ability to effectively convey complex scientific information to both internal and external stakeholders.Strong analytical and problem-solving abilities, with a strategic mindset.Ability to work in a fast-paced, dynamic environment and manage multiple priorities effectively.Preferably experience working in Big Pharma is a big plus

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