PV Case Processing Specialist Role

PV Case Processing Specialist – at ProPharma, Apply Now!

Are you passionate about drug safety and looking to make an impact in the pharmaceutical industry? ProPharma, the worldโ€™s largest Research Consulting Organization (RCO), is hiring a PV Case Processing Specialist. This role offers the chance to work on cutting-edge therapies while supporting global pharmacovigilance standards. If you have experience in adverse event case processing and a strong eye for detail, this opportunity might be your next career move.

About ProPharma

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the worldโ€™s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partnersโ€™ most high-profile drug and device programs.

Essential Functions

  • Responsible for daily case processing of adverse event cases (clinical trial and/or post marketed), including coding using MedDRA, determining seriousness and expectedness at the event and case level for Processing Specialist.
  • Perform case follow-up activities such as identification of information to be collected during follow-up.
  • Creating and reviewing case narratives.
  • Providing client notifications as required for case management.
  • Supporting and contributing to the development of training materials and training delivery.
  • Peer reviews of cases for quality, consistency, and accuracy as needed.
  • Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
  • Other duties as assigned as Processing Specialist.

Necessary Skills And Abilities

  • Strong verbal, written, and interpersonal communication skills.
  • High level of accuracy and attention to detail.
  • Ability to identify and resolve problems in a timely manner as Processing Specialist.
  • Able to work independently and collaboratively in a multi-disciplinary team.
  • Excellent organization and prioritization skills; able to multitask.
  • Basic knowledge of Pharmacovigilance.

Educational Requirements

Required: a Bachelor’s degree in life sciences.
Preferred: advanced degree, RN, RPh, PharmD, or equivalent.

Experience Requirements: Two years of related work experience.

APPLY ONLINE HERE

Keywords: PV Case Processing Specialist, ProPharma careers, pharmacovigilance jobs, adverse event case processing, MedDRA coding

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