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 Job #03074 Email this job to a friend
About our client
Our client is a leading privately held pharmaceutical company with operations in over 40 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 New Jersey
Salary
Highly competitive package, commensurate with experience
Responsibilities
1) Develop and implement product development strategies (initially in the urology therapeutic area)
2) Participate in other therapeutic areas (as derived from the company pipeline and/or in licensed development products)
3) Manage the conduct of clinical trials in the US with a strong component involving participation in global project development teams
4) Undertake all the duties normally associated with the execution of clinical trials
5) Establish clinical advisory boards in the areas of product development
6) Monitor safety and efficacy of any compound in development by the company
7) Participate in the safety monitoring and monitoring systems for clinical studies being managed by Clinical Research
8) Participate in cross-functional process-oriented activities (as required)
9) Develop medical efficacy and safety endpoints
10) Write protocol synopsis and full protocols (as required)
11) Contribute to the regulatory process during development and at regulatory submission
12) Interact with global marketing
13) Participate in publication planning, scientific meetings and advisory boards (as required)
14) Liaise with external scientists to plan and evaluate ongoing product development
15) Evaluate in-license projects (as requested)
16) Provide clinical guidance and training to staff
17) Participate in Investigator meetings (as required)
18) Work closely with international Project Development Teams
19) Ensure effective global development projects
20) Continuously improve management skills
Requirements
1) MD or equivalent with accreditation in a medical subspecialty (Urology, OB/GYN or Internal Medicine)
2) Minimum 3 years of experience in industrial pharmaceutical development or equivalent

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