Duties and Responsibilities
Design and develop clinical plans and protocols
Build relationships with principal investigators
Review clinical and scientific data
Contribute to key interactions with regulatory authorities
Develop clinical content for regulatory reports and CSRs
Provide regular updates on progress of clinical research
Required Qualifications
Graduate Degree: MD required
Prior experience with clinical trials
Ability to manage phase I-III clinical studies
Strong knowledge of drug development
Able to lead and collaborate in a team environment
Skilled in providing medical expertise to a cross functional team
Desired Qualifications
Specialty training in oncology or hematology