11 Medical Writing jobs in the Philippines
Scientist II Medical Writing
Posted today
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What Clinical Research contributes to Cardinal Health
Research is responsible for the development of new and improved products through initiating, designing, developing and executing research and product development projects.
Clinical Research is responsible for clinical operational and strategic consulting to provide innovative solutions, clinical development planning, protocols and clinical trials for all aspects of pharmaceutical, biologics and device development from initial clinical trials through post-approval maintenance. Incorporates integrated medical practice, disease state, therapeutic and compliance considerations with regulatory requirements across Phase 1 - 4 of the clinical development/clinical research continuum.
Qualifications
- 2-4 years of experience, preferred
- Bachelor's degree in related field, or equivalent work experience, preferred
What is expected of you and others at this level
- Applies working knowledge in the application of concepts, principles, and technical capabilities to perform varied tasks
- Works on projects of moderate scope and complexity
- Identifies possible solutions to a variety of technical problems and takes action to resolve
- Applies judgment within defined parameters
- Receives general guidance and may receive more detailed instruction on new projects
- Work reviewed for sound reasoning and accuracy
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.
Document Review Specialist II - Medical Writing
Posted 12 days ago
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Other
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer.
We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Summarized Purpose:**
We are excited to be growing our Medical Writing Functional Service Partnership (FSP) Team in APAC. We are seeking a Document Review Specialist II who will be dedicated to one or more clients in the FSP space, experience working in a range of document management systems would be preferred. As a remote-based Document Review Specialist within the FSP Team, you will review regulatory documents, including but not limited to submissions documents, protocols and amendments, clinical study reports, investigator's brochures, and patient safety narratives, to ensure quality standards and adherence to templates, client guidelines, editorial style guides, and industry standards. You will collaborate with internal clients, supporting and enabling effective communication and quality deliverables. This role requires meticulous attention to detail, a high English proficiency with the ability to communicate clearly and concisely, and understanding of regulatory document content.
**Key Responsibilities:**
+ Reviews highly technical scientific documents of all types developed within or outside of the company to ensure quality standards that meet or exceed client expectations.
+ Verifies scientific logic and clarity of the document by verifying data in tables, listings, and figures against source documents, checking for consistency according to current regulatory standards and guidelines.
+ Edits for accuracy, consistency, and grammatical correctness.
+ Adjusts schedule to accommodate unexpected requests for priority review.
+ Revises scientific language for usage, flow, clarity, and audience appropriateness.
+ Proactively queries authors to ensure compatibility with unique preferences and scientifically sound judgment.
+ Maintains, communicates, and applies knowledge of current guidelines, templates, and industry standards.
**Education and Experience:**
+ Bachelor's degree or equivalent and relevant formal academic/vocational qualification required.
+ Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).
+ Experience working in the pharmaceutical/CRO industry preferred.
+ If CRO experience: experience working in a client-dedicated role or with 1 to 2 clients over multiple projects
+ In some cases, an equivalency, consisting of a combination of appropriate education, training, and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
**Knowledge, Skills, and Abilities:**
+ Capable of focusing on document details and the overall objectives and intent of document messaging.
+ Good knowledge of the methods, techniques, and procedures of medical writing tasks.
+ Strong analytical ability.
+ Good working knowledge of medical terminology, statistical concepts, GCP, guidelines (e.g., ICH), and requirements of the FDA and other international regulatory agencies.
+ Attentive to detail and quality of documents, thorough and methodical.
+ Proficient oral and written communication and grammatical skills.
+ Good organizational and planning skills.
+ Good interpersonal skills.
+ Good knowledge and understanding of document management systems.
+ Proven ability to work effectively in a team environment.
+ Advanced computer literacy and expertise.
+ Capable of working well under pressure and remaining motivated.
+ Capable of working both independently and collaboratively with a team in a cross cultural, geographically dispersed environment.
**What We Offer:**
Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Scientific Writing Associate
Posted today
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Job Description
Work Location : Nuvali, Laguna
Onsite (3-6months)
Monday - Friday
RESPONSIBILITIES :
- Implementation and fulfillment of the safety manual's requirements.
- Implementation and
fulfillment of the personnel handbooks' requirements. - Implementation and fulfillment of the regulatory requirements.
- Acts as a role model in accordance with the Corporate Values of the company.
- Creation of study/publication summaries for the Study Database.
- Creation of study/publication summaries for scientific communication materials such as Scientific Reports.
Medical Writer
Posted today
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Job Description
Make Your Next Career Move and Defy Your Limits with KMC Solutions
At KMC Solutions, we make it easy for the world's fastest-growing companies to scale in the Philippines. As the country's leading provider of flexible office space and Employer of Record (EOR) services, we help businesses expand without the red tape—offering a faster and easier path to growth in the Philippines.
Position: Medical Writer
Location: BGC, Taguig, Metro Manila
Work Set-Up and Schedule: WFH/Remote and Dayshift (AU working hours).
About Our Client:
The client is a digital creative and technology business who fuse art and technology together, to create value through connected experiences and deliver exceptional services to their clients and customers globally.
Position Summary:
The Medical Writer will be responsible in developing medically and scientifically accurate communications for different audiences like healthcare professionals, patients and caretakers. This position requires a strong science or healthcare background combined with creative craft to produce content for branded campaigns, patient education materials, and medical slide decks.
Duties and Responsibilities:
• Translate complex medical/scientific concepts into clear and concise copy.
• Create medical slide decks, websites, branded campaign assets, and patient education materials.
• Drive the editorial process from first draft to final proof; ensuring accuracy and quality of all contents.
• Partner with design, strategy, account managers and project management teams
• Ensure all content is on-brand and Code-compliant
• Attend scientific meetings, advisory boards, and client meetings
• Contribute research and content to proposals and pitch presentations
• Stay up to date on current trends in medical education and/or pharma industry developments.
Qualifications:
• Preferably with a Bachelor's Degree or PHD in any science or medical field.
• At least 2-5 years of creating medical/science content and writing experience.
• Having pharma agency experience is a great advantage.
• Preferred but not required: Knowledge of Medicines Australia Code of Conduct
• Preferred but not required: Knowledge of using Veeva/PromoMats.
• Excellent English Communication Skills (both verbal and written).
• Proven ability of working within a multidisciplinary team.
• Ability to thrive in a fast-paced and collaborative work environment with an open mindset to learning and adapting quickly to any changes.
• Amenable to Work From Home.
• Amenable to Work in Dayshift (7AM to 4PM).
Medical Writer
Posted today
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Discover your 100% YOU with MicroSourcing
Position
: Medical Writer
Location
: WFH / Taguig
Work setup & shift
: WFH | Night shift
Why join MicroSourcing?
You'll Have
- Competitive Rewards: Enjoy above-market compensation, healthcare coverage on day one, plus one or more dependents, paid time-off with cash conversion, group life insurance, and performance bonuses
- A Collaborative Spirit: Contribute to a positive and engaging work environment by participating in company-sponsored events and activities.
- Work-Life Harmony: Enjoy the balance between work and life that suits you with flexible work arrangements.
- Career Growth: Take advantage of opportunities for continuous learning and career advancement.
- Inclusive Teamwork: Be part of a team that celebrates diversity and fosters an inclusive culture.
Your Role:
As a Medical Writer, You Will
- Analyze, gather, and document clinical requirements using best practices as defined by Clinical management.
- Validate clinical requirements including content requirements, in collaboration with subject matter experts (e.g., ClaimsXten experts, Certified coders, auditors, consultants, Medical Directors, etc.,) to guarantee correct coding guideline interpretations.
- Collaborate with Rule Writers team and cross-functional team members, to evaluate rule/policy behavior and to confirm that solution requirements meet business expectations and align with client implementation standards.
- Document content requirements to promote immediate post release content maintenance handoffs.
- Serve as a contributor to all user documentation (edit clarifications, Rules Guide, etc.,)
- Assist with all end-user training activities.
- Support Quality Assurance test plan validation.
- Perform user acceptance testing (UAT) of policies and/or rules.
- Provide requirements subject matter expertise to internal and external clients.
What You Need
Non-negotiables
- Bachelor's degree in health information management, Nursing or other Healthcare related degree required.
- American Academy of Professional Coders (AAPC) Certified Professional Coders (CPC) certification or American Health Information Management Association (AHIMA) Certified Coding Specialist-Physician (CCS-P) or Certified Coding Specialist (CCS) is required.
- 5 years or more relevant healthcare experience, with at least 2 years' experience as a payment/reimbursement or medical policy analyst, medical coder, medical claims processor, chart reviewer/auditor, or clinical editing analyst.
- 2 years or more' relevant experience with ClaimsXten solution.
- Effective communication skills: Must be an expert at presenting extraordinarily complex material via all mediums.
- Candidate must possess the ability to analyze complex data, identify trends and assess potential vulnerabilities.
- Superior critical thinking skills
- Proficiency in Microsoft applications.
Preferred Qualifications
- Knowledge of the Software Development Life cycle.
- Master's degree in healthcare related field.
- Knowledge of healthcare reimbursement and payment policies and methodologies.
- Working knowledge of pre-payment editing and payment integrity is preferred.
About MicroSourcing
With over 9,000 professionals across 13 delivery centers, MicroSourcing is the pioneer and largest offshore provider of managed services in the Philippines.
Our commitment to 100% YOU
MicroSourcing firmly believes that our company's strength lies in our people's diversity and talent. We are proud to foster an inclusive culture that embraces individuals of all races, genders, ethnicities, abilities, and backgrounds. We provide space for everyone, embracing different perspectives, and making room for opportunities for each individual to thrive.
At MicroSourcing, equality is not merely a slogan - it's our commitment. Our way of life. Here, we don't just accept your unique authentic self - we celebrate it, valuing every individual's contribution to our collective success and growth. Join us in celebrating YOU and your 100%
For more information, visit
- Terms & conditions apply
Medical Writer
Posted today
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A leading global pharmaceutical brand is seeking an experienced Medical Writer (Remote) to support a consensus initiative focused on molecular biomarker testing in late-stage hormone receptor-positive, HER2-negative breast cancer . The ideal candidate will have strong medical writing experience, particularly in consensus development within the APAC region, along with excellent project management skills.
- Conduct comprehensive literature reviews on molecular biomarkers in HR+/HER2– breast cancer.
- Draft evidence-based expert consensus statements in collaboration with Key Opinion Leaders (KOLs).
- Manage correspondence with KOLs, including coordination via iHCP platforms and handling of contracts.
- Maintain and track project timelines to ensure milestones and deadlines are met.
- Facilitate virtual meetings, including pre-meeting briefings and 2–3 consensus discussions.
- Manage end-to-end project delivery from literature review through to final submission.
- Develop the final publication manuscript and manage its submission to a peer-reviewed journal.
- Proven experience in consensus writing with a focus on the APAC region.
- Strong project management skills particularly in KOL engagement, including iHCP and contracts.
- Experience delivering end-to-end medical writing projects, from literature review through to journal submission.
- Excellent written and verbal communication skills, with the ability to effectively communicate with the client, medical experts, and other key stakeholders.
- Ideally with experience in oncologyor pathology.
Senior Medical Writer
Posted today
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Job Description
- Develop, review, and edit high-quality medical content across various formats: marketing materials, websites, brochures, and client-facing proposals
- Translate complex scientific data into clear, engaging, and accurate content tailored to target audiences
- Collaborate with internal teams and clients to ensure medical accuracy, compliance, and impactful storytelling
- Contribute to strategic discussions and help craft compelling narratives for healthcare brands
Qualifications
- Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field (Master's/PhD preffered).
- 8–10+ years of proven professional medical writing experience in pharmaceutical, healthcare, or clinical research organizations.
- Strong expertise in oncology and therapeutic areas is desired.
- Previous agency experience (marketing, website development, brochures, client-facing presentations/proposals).
- Excellent written and verbal communication skills with strong attention to details.
- Proficiency in MS Office (MSO).
- Comfortable working UK business hours.
- Ability to work onsite in Mandaluyong City.
- Amenable to work during weekends and Philippine holidays.
Work Setup: Onsite
Work Location: Pioneer Street, Mandaluyong City
Work Shifts: UK business hours
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Medical Writer Analyst
Posted today
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- Create, review, and refine high-quality medical content for a variety of formats including marketing collateral, websites, brochures, and client proposals.
- Ensure all written materials are scientifically accurate, clear, and aligned with industry standards.
- Collaborate with cross-functional teams to support project execution and contribute to strategic business development efforts.
- Act as a subject matter expert on medical and scientific content throughout the content development lifecycle.
- Bachelor's degree in Pharmacy, Medicine, or a related discipline; Master's or PhD is highly preferred.
- A minimum of 5–10 years of professional experience in medical writing within healthcare or clinical research settings.
- Strong grasp of medical terminology, clinical data interpretation, and regulatory guidelines.
- Exceptional written and verbal communication skills.
Medical Writer -Requirements
Posted 10 days ago
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Job Description
+ Analyze, gather, and document clinical requirements using best practices as defined by Clinical management.
+ Validate clinical requirements including content requirements, in collaboration with subject matter experts (e.g., ClaimsXten experts, Certified coders, auditors, consultants, Medical Directors, etc.,) to guarantee correct coding guideline interpretations.
+ Collaborate with Rule Writers team and cross-functional team members, to evaluate rule/policy behavior and to confirm that solution requirements meet business expectations and align with client implementation standards.
+ Document content requirements to promote immediate post release content maintenance handoffs.
+ Serve as a contributor to all user documentation (edit clarifications, Rules Guide, etc.,)
+ Assist with all end-user training activities.
+ Support Quality Assurance test plan validation.
+ Perform user acceptance testing (UAT) of policies and/or rules.
+ Provide requirements subject matter expertise to internal and external clients.
Required:
+ Education: Bachelor's degree in health information management, Nursing or other Healthcare related degree required.
+ American Academy of Professional Coders (AAPC) Certified Professional Coders (CPC) certification or American Health Information Management Association (AHIMA) Certified Coding Specialist-Physician (CCS-P) or Certified Coding Specialist (CCS) is required.
+ 5 years or more relevant healthcare experience, with at least 2 years' experience as a payment/reimbursement or medical policy analyst, medical coder, medical claims processor, chart reviewer/auditor, or clinical editing analyst.
+ 2 years or more' relevant experience with ClaimsXten solution.
+ Must be initiative-taking and self-directed,
+ Ability to work independently, with minimal direction.
+ Effective communication skills: Must be an expert at presenting extraordinarily complex material via all mediums.
+ Analytical skills: Candidate must possess the ability to analyze complex data, identify trends and assess potential vulnerabilities.
+ Superior critical thinking skills
+ Proficiency in Microsoft applications.
Preferred Qualifications:
+ Knowledge of the Software Development Life cycle.
+ Master's degree in healthcare related field.
+ Knowledge of healthcare reimbursement and payment policies and methodologies.
+ Working knowledge of pre-payment editing and payment integrity is preferred.
Medical Writer - Requirements
Posted 17 days ago
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Job Description
+ Analyze, gather, and document clinical requirements using best practices as defined by Clinical management.
+ Validate clinical requirements including content requirements, in collaboration with subject matter experts (e.g., ClaimsXten experts, Certified coders, auditors, consultants, Medical Directors, etc.,) to guarantee correct coding guideline interpretations.
+ Collaborate with Rule Writers team and cross-functional team members, to evaluate rule/policy behavior and to confirm that solution requirements meet business expectations and align with client implementation standards.
+ Document content requirements to promote immediate post release content maintenance handoffs.
+ Serve as a contributor to all user documentation (edit clarifications, Rules Guide, etc.,)
+ Assist with all end-user training activities.
+ Support Quality Assurance test plan validation.
+ Perform user acceptance testing (UAT) of policies and/or rules.
+ Provide requirements subject matter expertise to internal and external clients.
Required:
+ Education: Bachelor's degree in health information management, Nursing or other Healthcare related degree required.
+ American Academy of Professional Coders (AAPC) Certified Professional Coders (CPC) certification or American Health Information Management Association (AHIMA) Certified Coding Specialist-Physician (CCS-P) or Certified Coding Specialist (CCS) is required.
+ 5 years or more relevant healthcare experience, with at least 2 years' experience as a payment/reimbursement or medical policy analyst, medical coder, medical claims processor, chart reviewer/auditor, or clinical editing analyst.
+ 2 years or more' relevant experience with ClaimsXten solution.
+ Must be initiative-taking and self-directed,
+ Ability to work independently, with minimal direction.
+ Effective communication skills: Must be an expert at presenting extraordinarily complex material via all mediums.
+ Analytical skills: Candidate must possess the ability to analyze complex data, identify trends and assess potential vulnerabilities.
+ Superior critical thinking skills
+ Proficiency in Microsoft applications.
Preferred Qualifications:
+ Knowledge of the Software Development Life cycle.
+ Master's degree in healthcare related field.
+ Knowledge of healthcare reimbursement and payment policies and methodologies.
+ Working knowledge of pre-payment editing and payment integrity is preferred.