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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #03085 Email this job to a friend
About our client
Our client is a rapidly growing biotech company headquartered in Minnesota that is focused on the development and commercialization of therapeutics for oncology indications. The company has marketed products to support ongoing development, an experienced management team and board and an empowering corporate culture that is focused on the professional development of its employees. This is a great opportunity for the right candidate.
Position Location
Medical Director Minnesota
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Provide medical and scientific support to the company's clinical development efforts in various oncology projects
2) Develop strategy as well as the design, conduct, analysis and reporting of Phase 1 – 3 studies
3) Provide medical expertise and leadership to clinical and non-clinical activities of the Pharma Group
4) Evaluate and assess, along with senior pharma leaders, exploratory indications and market potential of compound
5) Draft clinical development plans for the company's proprietary compound
6) Conceive study designs, draft protocol synopses and guide protocol writing
7) Oversee safety-monitoring activities including data safety monitoring boards
8) Evaluate clinical/safety data generated by studies
9) Present clinical data/findings (as required) at internal/external/regulatory meetings
10) Work with cross-functional team members to facilitate data management, statistical analysis and medical writing
11) Interact with participating clinical investigators at US/EU/Asian sites
12) Prepare and/or review regulatory submissions from clinical and safety aspect including INDs, annual reports, CSRs and BLAs
13) Conduct/participate on internal marketing/licensing teams
14) Develop and foster outside relationships with key opinion leaders, collaborating researchers and research sites
Requirements
1) Medical degree from an accredited institution
2) Medical Oncology Board eligibility/certification
3) Minimum 4 years of relevant pharmaceutical/biotech experience in a similar role (drug safety or clinical research)
4) Superb communication skills (verbal and written)
5) Excellent problem-solving and interpersonal skills
6) Willingness to travel (minimal – with some international travel)

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