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Sterling Life Sciences, Specialists in Pharmaceuticals, Healthcare and BioTech Recruitment
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 Job #03124 Email this job to a friend
About our client
Our client is a privately held biotechnology company with operations in over 20 countries. With marketed products, an experienced management team, 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 Connecticut
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Handle medical monitoring of clinical trials
2) Provide scientific and medical expertise for clinical trials as well as consulting projects
3) Act as a medical resource for staff members
4) Review and manage Serious Adverse Events (SAEs) during clinical trials
5) Participate in management of SAEs
6) Interact with the FDA and participate in advisory boards
7) Participate in developing and reviewing scientific writing projects
8) Develop and review study protocols, study reports, manuscripts, FDA briefing documents and regulatory analyses
9) Create and conduct employee training/continued education
10) Attend capabilities presentations and make client visits (as needed)
11) Identify potential areas of business development and client expansion
12) Manage international clinical projects
Requirements
1) MD
2) Minimum 5 years of hematology, oncology or immunology sub-specialty experience
3) 3 years of pharmaceutical, biotech industry or CRO experience a plus
4) Experience in leading clinical and cross-functional teams
5) Knowledge of GCP and ICH guidelines
6) Willingness to travel primarily to Asian countries (up to 50%)

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