Director Clinical Development

Performs all job responsibilities in accordance with standards of Good Clinical Practice. Delegates study responsibilities as appropriate to trained study staff Possesses a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form. Reviews all protocols prior to acceptance at the site for feasibility. Reviews Investigator's Brochure prior to performing any study related activities. Ensures informed consent has been obtained prior to performing any study procedures. Participates in Sponsor dose escalation meetings and other safety discussions with the Medical Monitor. Performs all study responsibilities in compliance with the IRB approved protocol. Reviews screening documentation and approves subjects for admission to study. Reviews and evaluates all study data and comments to the clinical significance of any out of range results.

According to JobzMall, the average salary range for a Director Clinical Development in Miramar, FL, USA is between $154,850 and $224,831 per year.

This figure is an average taken from various sources, and is based on the median salary of the job. The exact salary range may vary depending on the experience and qualifications of the individual, as well as the company they are working for. Factors such as location, size of the company, and industry can also affect the salary range.

Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).