What are the responsibilities and job description for the PV Case Processing Specialist position at ProPharma Group?
Job Description
ProPharma is the world's largest Research Consulting Organization, partnering with clients across the product lifecycle through an advise-build-operate model.
Essential Functions:
- Process adverse event cases, including coding using MedDRA and determining seriousness and expectedness.
- Perform case follow-up activities, such as identifying information to be collected during follow-up.
- Create and review case narratives, providing client notifications as required.
- Support training material development and delivery, highlighting areas of concern or discrepancies.
- Maintain up-to-date knowledge of global safety regulations for medicines.
- Peer-review cases for quality, consistency, and accuracy.
- Perform other duties as assigned.
Necessary Skills and Abilities:
- Demonstrate strong verbal, written, and interpersonal communication skills.
- Show a high level of accuracy and attention to detail.
- Be able to identify and resolve problems in a timely manner.
- Work independently and collaboratively in a multi-disciplinary team.
- Exhibit excellent organization and prioritization skills, with the ability to multitask.
- Have basic knowledge of Pharmacovigilance.
Requirements:
- Bachelor's degree in life sciences.
- Advanced degree, RN, RPh, PharmD, or equivalent preferred.
Experience:
- Two years of related work experience.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion, and provide a safe space where all employees feel empowered to succeed.
