Pharmacovigilance Jobs at ProPharma Group | BS Life Science Candidates Apply Now
Are you an experienced life sciences professional with a passion for pharmacovigilance and drug safety? ProPharma Group, a trusted global partner to biotech, pharmaceutical, and medical device companies, is hiring a PV Specialist โ Case Processing in the United States. This 12-month full-time role offers the opportunity to work on adverse event case management, contribute to clinical research safety, and ensure compliance with global regulatory standards while advancing your career with a leading consulting organization.
About ProPharma Group
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. 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.
Job Description
Job Post: PV Specialist, Case Processing
Location: United States
Time Type: Full-time
Job Requisition ID: JR 7924
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.
12-month temporary position
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.
- Perform case follow-up activities, such as the 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.
- Highlight areas of concern/discrepancies to the Principal PV Specialist, Case Processing, and/or Manager, Case Processing when related to ICSRs.
- Acquire and maintain an up-to-date knowledge of global safety regulations for medicines.
- Peer reviews of cases for quality, consistency, and accuracy as needed.
- Other duties as assigned.
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 promptly.
- Able to work independently and collaboratively in a multi-disciplinary team.
- Excellent organization and prioritization skills; able to multitask.
- Basic knowledge of Pharmacovigilance.
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. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.
Keywords: PV Specialist, Case Processing skills, ProPharma Group, pharmacovigilance, clinical research, consulting solutions, Job Posting
