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Pharmacovigilance Associate Lead

1 month ago


Durham, North Carolina, United States Lifelancer Full time
About the Role

We are seeking an experienced Pharmacovigilance Associate Lead to join our team. This role is responsible for collecting, processing, evaluating and reporting of incoming Serious Adverse Event (SAE) data.

Job Description
  • Author Safety Management Plans for assigned studies
  • Attend internal and client meetings as appropriate
  • Review incoming SAE data for completeness and accuracy
  • Perform data entry in the Safety Database
  • Generate queries for missing or unclear information and follow-up with sites for resolution

In this role, you will serve as a lead on moderate to large-sized studies that are moderate to complex in scope of work. You will have moderate support from senior staff and be responsible for tasks such as attending investigator meetings, presenting at meetings, reviewing SAE data, performing data entry, generating queries and maintaining knowledge of safety related regulations.

Requirements
  • Minimum of 3 years of pharmacovigilance experience
  • Bachelor's degree in science related field or equivalent combination of relevant education and experience
  • Computer literacy and strong working knowledge of MS Office applications
About Us

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Why Choose Us?

We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.