Clinical Research Medical Director - Oncology

Benefits

Qualifications

• •MD or DO degree from an accredited medical school
• •2 years of clinical research experience and/or basic science research

Responsibilities

• •In this vital role you will support Clinical Development in Prostate cancer
• •Supporting the development, execution and communication of the global scientific/medical evidence plan
• •Supporting cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
• •Supporting the development of key scientific external relationships with opinion leaders
• •Participating and providing clinical input into safety and regulatory interactions
• •Provide clinical/scientific input during the development and execution of clinical trials
• •Interpret clinical trial data
• •Participate in safety assessments
• •Participate in interactions with regulatory agencies
• •Author CSRs, publications and regulatory submissions
• •Develop key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Leader
• •Identify new clinical research opportunities
• •Support in-licensing and out-licensing activities and partner relationships
• •Support product lifecycle management for new indications as directed by Global Development Leader
• •Provide clinical content input to:
• •Regulatory interactions and documents
• •Safety interactions and documents
• •Materials to be used in Scientific Affairs
• •Materials to be used by the Commercial Organization
• •16 more items(s)