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Senior Manager / Medical Writing

2+ years
Not Disclosed
10 May 23, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Manager / Medical Writing
Location: Manila, Philippines
Category: Consulting
Job Type: Full Time
Posted Date: May 22nd, 2025
Job ID: R257321
Estimated Salary: PHP 1,800,000 – PHP 2,400,000 per annum (estimated)


About Cencora

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures. Every person here is essential to delivering on that purpose. Join our innovative company and help improve the lives of people and animals everywhere.


Job Details

Role Summary:
This role involves preparing technical documentation such as Literature Reviews, Clinical Performance Reports, and EQA Analysis Reports in line with European In Vitro Diagnostics Regulations. Ideal candidates have strong medical writing expertise with experience in immunohistochemistry and cancer diagnostics preferred.

Job Description:

  • Prepare technical documentation for In Vitro Diagnostic (IVD) medical devices per European IVD Regulations and country-specific regulatory requirements.

  • Draft performance evaluation plans, analytical performance reports, clinical performance reports, and scientific validity reports.

  • Prepare declarations of conformity and summaries of safety and performance for IVD devices.

  • Develop checklists for standard assessments of legacy devices to identify required regulatory updates.

  • Prepare labelling documents according to country-specific guidelines.

  • Conduct and review systematic literature searches for scientific and medical documents.

  • Review documents related to technical specifications, product design, and performance reports for IVD products and medical devices.


Required Skills:

  • Strong background in In Vitro Diagnostics, preferably from clinical affairs or as a Technical Documentation reviewer within a European Notified Body.

  • Knowledge of Companion Diagnostics.

  • Expertise in External Quality Assessment (EQA) schemes and report analysis.

  • Experience in immunohistochemistry.

  • Proficiency in clinical/medical writing, particularly for performance evaluations and clinical performance reports.

  • Expertise in statistics.

  • Experience in therapy areas such as cancer diagnostics.

  • Experience managing in-house and/or external clinical studies.


What Cencora Offers

Benefit offerings outside the US vary by country and align with local market practices. Eligibility and effective dates may differ for team members covered by collective bargaining agreements.


Affiliated Company: DRA Consulting Oy

Equal Employment Opportunity:
Cencora is committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status, or other protected classes. Harassment is prohibited, and all recruitment, training, compensation, benefits, promotions, and transfers comply with non-discriminatory principles. Reasonable accommodations are provided for individuals with disabilities upon request.

For accommodation requests during the employment process, please call 888.692.2272 or email hrsc@cencora.com. Only accommodation-related messages will receive a response.