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Drug Safety Associate

United States of America, Remote
Additional Locations: Remote - United States of America
Job ID R0000015078

Category Medical Sciences

ABOUT THIS ROLE

Parexel is looking for a Drug Safety Associate with drug safety case processing experience to join our team in North America!

The Drug Safety Associate will provide technical and process-related support to drug safety management (clinical trial and post-marketed), ensuring compliance with relevant regulations and Standard Operating Procedures (SOPs).

Key Accountabilities:
Global Pharmacovigilance Processing Group (GPPG):

  • Assist in development of project-specific safety procedures, workflows, and templates.

  • Assist in project-specific safety database setup, development of data entry guidelines, and user acceptance testing

  • Triage incoming reports for completeness, legibility, and validity

  • Electronic documentation and quality control of drug safety information

  • Data entry of case reports into safety database / tracking system

  • Request follow-up and perform query management

  • Coding of data in the safety database

  • Writing case narratives

  • Create and maintain project-specific working files, case report files and project central files

  • Assist with additional Drug Safety Specialist and/or Safety Service Project Leader (SSPL) activities, as required

  • Inform Line Manager (LM)/Team Manager, Safety Services Project Leader (SSPL) or Project Leader (PL) and Regional Head of PV Operations of potential change-in-scope of projects

  • Participate in client and investigator meetings, as required

  • Attend internal, drug safety and project-specific training sessions

  • Perform literature searches

  • Preparation for, participation in, and follow-up on audits and inspections

  • Delegate work as appropriate to Drug Safety Assistants

Skills:

  • Analytical and problem-solving skills

  • Able to perform database/literature searches.

  • Excellent interpersonal skills, verbal / written communication skills

  • Excellent organizational and prioritization skills

  • Ability to work collaboratively and effectively in a team environment.

  • Client focused approach to work

  • Experience with computer applications


Knowledge and Experience:

  • Related experience gained in a drug development and/or healthcare environment is an advantage.

  • Ideal candidate will have at least 2- 3 years of recent Argus case processing experience, along with 1-2 years of clinical trial case processing experience desired.

  • AT LEAST 3+ year of recent Post-Marketing experience preferred.

Education:

  • Degree in Pharmacy, Nursing, Life Science, or other health-related field, or equivalent qualification/work experience

  • Associates/diploma degree in any of the above with appropriate work experience


#LI-REMOTE

EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

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CEO of Parexel
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Jamie Macdonald
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We Care Everything we do has the potential to impact patient lives. We show we care by taking our work seriously, demonstrating empathy and acting with heart. Our overarching Guiding Principle that sits across our four core values and translates ...

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DATE POSTED
December 24, 2023

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