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Pharmacovigilance Associate - RPH/PHRN (Voice) | ONSITE | Start ASAP!

2022-10-20 07:21IP Location 菲律宾1600
Area:Metro Manila (NCR) Taguig
Industry Category:Healthcare
Position:Practitioner / Medical Asst
Department:
Number Of Recruits:several
Nature Of Work:Full Time
Gender Requirements:Male
Marriage Requirement:No marital status restrictions
Education Level: Bachelor's Degree
Work Experience:No work experience restrictions
Age:Above 18 years old
Salary Package:Negotiable
RESPONSIBILITIES:Identify and collect adverse event information and complete the in-take of a Pharmacovigilance Safety Report in Client Safety Systems through a thorough telephonic patient assessment and evaluation of information.Ensure scientific rigor through accurate, complete and consistent data entry of medical information through numerous adverse event reports and notes with emphasis on timeliness and quality in order to meet regulatory demands.Review and evaluate case information for medical completeness and accuracy prior to the appropriate completion of processing through pushing, triaging or escalation of all AE reports within a rigid regulatory mandated timeframe.Respond to medical information requests using approved resources and documentation in Client medical information systems.Identify product quality and device complaints and document in Client s product/device complaint systems.Compliance with departmental guidelines, SOPs, ongoing training, and regulatory guidelines.Effectively communicate by actively listening to acquire information and understand another’s viewpoint to communicate clearly and establish rapport with customers, colleagues, and interdepartmental groups.Strong verbal communication skills with external and internal customers.Prepare and communicate timely and accurate information with customers using various platforms.Understands and assimilates information to accurately respond to situations by providing fair and unbiased scientific data to customers.Completes follow up reports and response documentation in a timely, concise, and objective manner.Use of multiple databases to document adverse event, medical information, and product complaint information.Identify and communicate possible issues to Team Leaders and Manager.May assist in training others on specific, non-complex, process or database.Co-ordinate with team on problem solving and improvement initiatives.Responsible for completion of day-to-day work and process flows within the agreed service levels (SLAs).QUALIFICATION(S):Required –Registered Nurse or Pharmacist with a minimum of 6 months' experience.Registered Nurse/Pharmacist with acute and inpatient bedside experience is preferred.Bachelor or Master of Nursing/Pharmacy is preferred.Excellent clinical judgment and ability to interpret, synthesize and communicate clinical information and safety data in a scientifically sound and understandable way.Strong knowledge of medical terminology, pharmacology, human body systems and disease processes,Basic knowledge of general principles of adverse events, product quality, medical information, and Food and Drug Administration (FDA) regulations.Expert clinical assessment skills with the capacity to triage calls and circumstances appropriately.Robust critical thinking and analytical skills with the ability to make prompt high-level decisions.Ability to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas.Experience working with Pharma company; (healthcare experience will be considered too).Contact center experience with inbound/outbound voice programs involving patient and health care providers (Preferred).
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