Director Clinical Development
Miramar, FLFull-time
154,850–224,831 a year
Behavioral Health Market Context
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Job Description
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.
Teva Pharmaceutical USA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Teva Pharmaceutical USA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Qualifications
Benefits
Responsibilities
- •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
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