Senior Medical Director

Responsibilities:

• Assist in design, author and/or review clinical study synopses, protocols, amendments, study reports and other study-related documents.
• Act as a medical monitor for assigned study.
• Discuss study design with investigators and key opinion leaders.

Qualifications:

• Medical Doctor (MD) with experience in solid tumor clinical trials required; recent experience in breast carcinoma preferred.
• Thorough working knowledge / understanding of clinical trial design, methodology and statistical concepts.
• Working knowledge of the IND/NDA process.

Preferred:

• Leadership skills include a collaborative and team-oriented approach.
• Ability to build strong relationships with co-workers of various backgrounds and expertise.
• Ability to function at a high level in a team setting whether leading the group or acting as an individual contributor.