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| Job #03073 |
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| 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 |
| Associate Director, Clinical Research |
New Jersey |
| Salary |
| Highly competitive package, commensurate with experience |
| Responsibilities |
1) Prepare clinical protocols 2) Handle clinical trial initiation as well as management and medical monitoring in the orthopedic therapeutic area 3) Support all activities related to the clinical product development programs 4) Report to the Executive Medical Director 5) Study planning and design 6) Handle clinical protocol preparation and implementation 7) Initiate, coordinate enrollment and monitor clinical studies (Phase I – IIIb) 8) Manage the clinical data analysis and interpretation of clinical results 9) Report and fill data from clinical development studies (Phase I – IIIb) 10) Report periodic and annual drug safety 11) Prepare presentations on clinical development plans, project progress updates and clinical data 12) Prepare and participate in advisory board meetings as well as investigators meetings 13) Participate in multidisciplinary projects designed to support new drug development or commercialization of existing products |
| Requirements |
1) MD 2) 1 – 3 years of experience in pharmaceutical industry or related experience 3) Good track record in clinical project management in the area of orthopedics, rheumatology and internal medicine 4) Clinical and scientific expertise in preparing clinical documents and/or publications 5) Ability to organize, analyze and interpret clinical and scientific data 6) Commitment to team work 7) Ability to provide leadership by example |

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