Large pharmaceutical company is seeking a Clinical Study Director reporting to the Director of Clinical Operations. This a 6-9 month contract position that may become a full time opportunity. The selected candidate can work from either the New Jersey or eastern Pennsylvania sites. There may be some flexibility in the number of days per week on site, but the individual will need to be close to the sites in order to interact with Clinical Trial Team members. The role is key for medical supervision and medical management of clinical trials proposed or to be performed by the Clinical Science and Operations Platform CSO of the company RD. The Clinical Study Director CSD is the medical reference in the clinical study and other clinical activities. The CSD will provide appropriate medical input and support for all of these clinical activities. He/she will provide medical training and medical information to study teams and support for all Units CSUs and investigators. He/she will be deeply involved in the feasibility process; will be accountable for medical review and will collaborate and interact with Pharmacovigilance to review safety data. The CSD will also interact with Medical Advisors in CRUs or Clusters. A specialization in Neurology is preferred to better serve some customers. Qualifications include: MD degree; qualification in a medical specialization, especially neurology; previous experience in clinical research and/or Drug Development and/or Pharmacovigilance; knowledge in ICH, GCP and local regulations; Fluent in English writing and speaking. Salary is negotiable. If you are interested in this position, please send resume in Word format as an attachment to Beverly Slomka at bslomka@staffpointe.com. Find more opportunities online or register for free at www.staffpointe.com. Only qualified candidates with an MS Word attached resume and recent, relevant healthcare experience will have their resumes considered. Please refer to job# BSX1663
