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Job Description
Perform activities related to interim analysis and data base lock e.g. data cleaning clinical data review. Analyze and interpret study data and support preparation of reports for the FDA. Proactively provide feedback on emerging clinical and competitive trends.
Qualifications
ESSENTIAL DUTIES AND RESPONSIBILITIES:Education: BSN, MSN, Pharm.D., PhD or M.D. in related discipline and five or more years of related experience, or; Equivalent combination of education and experience.
Position Requirements: Extensive experience cleaning data Experience with preparing clinical study reports Hepatocellular Carcinoma and or other solid tumor research experience preferred but not mandatory Thorough understanding of clinical trial design, in Oncology preferred and all aspects of the drug development process is essential Five plus years Pharmaceutical experience preferred. Experience in activities related to interim analysis and data base lock e.g. data cleaning / clinical data review (may include experience with writing or reviewing safety narratives) Experience with EDC systems (e.g., InForm preferred)
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Additional Information
DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
Vacancy expired!