Senior Pharmacovigilance Coordinator, Case Processing

ProPharma Group; Makati; On-site; PHP 390,600 - 837,000; Full time

Job summary

ProPharma Group in Makati City seeks a Senior Pharmacovigilance Coordinator to oversee case processing, from intake to data entry, ensuring accuracy and regulatory compliance. You will redact PHI, perform literature-related tasks, and prepare draft reports for client review.

The role emphasizes strong communication, meticulous attention to detail, and teamwork, with hybrid work options and opportunities for professional growth within a global pharmacovigilance framework.

Qualifications

• Bachelor's Degree in Life Science, Pharmacy, or Nursing is required.

Responsibilities

• Manage assigned mailboxes and triage client communications; screen and redact PHI; enter basic data into safety database; oversee team workload to meet daily/weekly goals.

Skills

Communication skills

Organizational skills

Attention to detail

Independent work

Education

Bachelor's Degree in Life Science/Pharmacy/Nursing

Job description

## Senior Pharmacovigilance Coordinator, Case ProcessingApplylocations: Makati Citytime type: Full timeposted on: Posted Yesterdayjob requisition id: JR 10195For the past 25 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.**Essential Functions:*** 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.* Help oversee team workload and client deliverables to make sure that daily/weekly goals are hit by the collective intake team as needed.* Other duties as assigned.**Necessary Skills and Abilities:*** Strong verbal, written and interpersonal communication skills.* Proficient computer knowledge and computer keyboarding skills.* Strong organization and prioritization skills, with strong attention to detail.* Ability to work independently and within in interdisciplinary a team.**Educational Requirements:*** Bachelor's Degree in Life Science, Pharmacy, or Nursing**Experience Requirements:*** Required: one year of related work experience.* Preferred: one year of industry experience.#LI-FDT1We 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.\*\*\*