Pharmacovigilance Coordinator, Case Processing

Posted 4 Days Ago
Be an Early Applicant
Hiring Remotely in United States
Remote
Entry level
Healthtech • Consulting • Pharmaceutical
The Role
Monitor and triage pharmacovigilance inboxes, perform case book-in and duplicate searches, redact PHI, facilitate literature activities, triage regulatory database searches, prepare draft reports, and enter basic (and, with training, full) case data into the safety database.
Summary Generated by Built In

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 partners’ most high-profile drug and device programs.

The Pharmacovigilance (PV) Coordinator, Case Processing, monitors and triages the communications received via the PV inbox. The Coordinator performs data entry of (Clinical & Post-Marketing) cases received via email or fax. The Coordinator generates and distributes deliverables from the safety database as assigned in accordance with the safety management plan and maintains distinctive quality and commitment as the operating philosophy in carrying out all processes. The Coordinator continually seeks out ways to enhance customer service experience both internally and externally.

  • Manage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications.

  • Perform Duplicate searches and complete initial book-in as required.

  • Screen and redact the source documents for PHI as per company procedures.

  • Facilitate literature related activities as needed.

  • Initial triage of regulatory authority database searches.

  • Send draft reports to clients for review as needed.

  • Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event.

  • As applicable perform full data entry into safety databased with proper experience and training.

  • Other duties as assigned.

#LI-KP1

#LI-REMOTE

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.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
Bozeman, MT
2,059 Employees
Year Founded: 2001

What We Do

ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies.

With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science

Similar Jobs

ServiceNow Logo ServiceNow

Consultant

Artificial Intelligence • Cloud • HR Tech • Information Technology • Productivity • Software • Automation
Remote or Hybrid
New York, NY, USA
28000 Employees

SambaSafety Logo SambaSafety

Mid-market Account Executive

Insurance • Logistics • Software • Transportation • Business Intelligence
Remote or Hybrid
United States
300 Employees
80K-160K Annually
Remote or Hybrid
5 Locations
205000 Employees
37K-66K Hourly

Airwallex Logo Airwallex

Senior Back-end Engineer

Artificial Intelligence • Fintech • Payments • Business Intelligence • Financial Services • Generative AI
Remote or Hybrid
San Francisco, CA, USA
2000 Employees

Similar Companies Hiring

Camber Thumbnail
Social Impact • Healthtech • Fintech
New York, NY
53 Employees
Sailor Health Thumbnail
Telehealth • Social Impact • Healthtech
New York City, NY
20 Employees
Granted Thumbnail
Mobile • Insurance • Healthtech • Financial Services • Artificial Intelligence
New York, New York
23 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account