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    • Assists with writing custom medical information responses utilizing this data.
    • Working knowledge of medical terminology, pathophysiology, pharmacology,…
    • View all ProPharma Group jobs - Makati jobs - Information Specialist jobs in Makati
    • Salary Search: Medical Information Specialist, Philippines salaries in Makati
    • Basic familiarity with medical terminology.
    • Work Schedule:* On-site (Flexible / Selected Days / Clinic Hours).
    • Willing to work on a part-time schedule.
    • Experienced working in blood center is an advantage.
    • Perform various laboratory examinations on collected blood as mandated by the Department of Health on all…
    • Reimbursement of medical expenses up to Php 17,700 per month, capped at Php 177,000 per year, for eligible medical-related expenses.
    • 8-hour shift per day.
    • The Admission Associate is responsible for processing patient admission.
    • Assigns Bed base on patient preference, availability and patient case.
    • Experienced working in blood center is an advantage.
    • Perform various laboratory examinations on collected blood as mandated by the Department of Health on all…
  • View similar jobs with this employer
    • Welcome and introduce clients to the skin center.
    • Work with the team to create a positive center atmosphere and maintain its quality.
    • Preferably College Graduate in Medical allied.
    • With knowledge in Healthcare Service is a plus.
    • Collects necessary medical information before consultations (e.g., symptoms, allergies, medical history, and laboratory results).
    • Deliver quality basic nursing care under the supervision of the Head Nurse, Charge Nurse, or Staff Nurse.
    • Assist in the admission, transfer, discharge, and…
    • With or without related experience.
    • Willing to work in Pasig City.
    • Job Types: Full-time, Permanent.
    • Technical Knowledge: Basic understanding of medical terms, triage processes, and prior experience with PhilHealth administration.
    • Maintain the confidentiality of patient information and medical records.
    • Experience in medical encoding, laboratory, clinic, or hospital settings is an…
    • Handles customer inquiries or any non-medical concerns within various channels;
    • Offers training program to provide international standard service.
    • Reviews and checks PHIC and OWWA forms for transmittal.
    • Processes forms and patients for direct filing of claims to PHIC due to late submission.

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Job Post Details

Medical Information Specialist, Philippines - job post

ProPharma Group
3.3 out of 5 stars
Makati
You must create an Indeed account before continuing to the company website to apply

Job details

Job type

  • Full-time

Location

Makati

Full job description

For 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.

The Medical Information Specialist (MIS) position is part of the ProPharma Medical Information Contact Center and follows all corresponding regulations, industry standards, and client/internal policies regarding medical information and the collection and documentation of adverse events, special situation events, and product complaints.

Essential Functions Include:Medical Information service delivery
  • Responds to unsolicited consumer, health care professional and other external customer requests for medical and safety information received via telephone, website/e-mail, letter, fax, and scientific meetings on behalf of ProPharma’ s pharmaceutical clients.
  • Provides labeled and unlabeled medical/safety information responses in accordance with regulatory requirements, industry standards and client and ProPharma internal policies and practices.
  • Accurately identifies, documents and reports adverse events, pregnancy reports, special situation events and product complaints in a clear and concise manner per government regulations, ProPharma Standard Operating Procedures (SOPs) and client Working Practices (WPs).
  • Ensures tasks are completed within the deadlines documented in the agreed ProPharma SOPs and WPs.
  • Formulates and provides accurate responses utilizing approved labeling and company standard responses, published literature and other data. Assists with writing custom medical information responses utilizing this data.
  • Logging all enquiries handled in an accurate, comprehensive, and timely fashion into Inquiry Handling Systems. Quality Assurance
  • Maintains quality in all areas of the job, including performing quality checks on Adverse Events, Product Quality Complaints, correspondence, and enquiries logged into the Inquiry Handling Systems General
  • Provides after-hours coverage on a rotated basis subject to business requirements.
  • Adheres to company and country-specific privacy policies, ensuring any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations described in ProPharma SOPs and the Confidentiality Statement within the Contract of Employment.
  • Complies with the Company’s health and safety policies.
  • Other activities as assigned as delegated by the Manager.

Qualified candidates must have:
  • Life science degree OR Nursing degree (RN/BS/BA/MS) OR Pharmacy degree
  • Excellent verbal and written communication skills, including proofreading, professional telephone etiquette and empathetic customer service skills.
  • Ability to write in a fluent and grammatically correct manner in the target language for the role
  • English language proficiency. Japan-based roles only: TOEIC 800=<
  • Working knowledge of medical terminology, pathophysiology, pharmacology, regulations and industry standards.
  • Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability.
  • Ability to multitask with attention to detail within restrictive timeframes, including sound planning, prioritizing and organizational skills.
  • Proactive with demonstrative ability to independently identify problems and suggest effective solutions.
  • Ability to learn, take instruction and apply to daily operations/tasks.
  • Receptive to constructive feedback and able to take responsibility for work allocated.
  • Self-motivating. Ability to demonstrate initiative and internal drive. Willingness to seek out additional workload projects.
  • Effectively work independently and as part of a team.
  • Highly proficient in computer applications, including Microsoft Office software platforms and Adobe Acrobat, and experience using a document management system. Aptitude to learn other computer systems including inquiry handling database.

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.***

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