Quick Summary
Key Responsibilities
Performs tasks according to the assigned medical writing activities including systematic literature reviews primarily for the generation of Clinical Evaluation Reports (CER),
Requirements Summary
data processed fairly, transparently, and lawfully; collected for specified and legitimate purposes; adequate, relevant,
Technical Tools
Other
Responsibilities
~2 min read- →Performs tasks according to the assigned medical writing activities including systematic literature reviews primarily for the generation of Clinical Evaluation Reports (CER), Summary of Safety and Clinical Performance (SSCP), State of the Art (SOA), Post-Market Surveillance (PMS) including Periodic Safety Update Reports (PSUR), and Premarket Approval (PMA) Food and Drug Administration (FDA) Reports, including Humanitarian Device Exemption (HDE), Investigative Device Exemption (IDE) Reports, and Health Economics and Market Access (HEMA) research. The specific tasks are to be determined based on the assigned role in the project.
- →Supports review of work done by peer teammates, on need basis
- →Alerts and escalates to senior members as required, whenever project deliverable risks are visualized, OR issues are encountered impacting the delivery schedule
- →Ensures error-free and acceptable quality of assigned deliverables
- →Responsible for ensuring training compliance and timesheet compliance
- →Ensures that all assigned goals (e.g., utilization and efficiency) are met as per set standards for the performance year
- →Follows and complies with the Company’s Code of Conduct, Policies, and Procedures
- →Responsible for confidentiality, integrity, availability, and safeguarding of data
- →Responsible for reporting of security incidents and PIMS breaches as applicable
- →Complies with company QMS, ISMS, and PIMS requirements and applicable regulatory requirements
- →Demonstrates adherence and compliance to PIMS/GDPR requirements as follows: data processed fairly, transparently, and lawfully; collected for specified and legitimate purposes; adequate, relevant, and limited to the specified purposes; processed in a secure manner
Requirements
~1 min read- At least 1-3 years of experience in medical writing, or any related field as applicable
- Can work in a diverse team environment
- Good analytical and comprehension skills
- Proficient in time management and can work with minimal supervision,
- Proficiency in oral and written English language
- Proficiency in Microsoft Office Suites (e.g. Word, Excel, PPT, SharePoint).
- Minimum bachelor’s degree in any life sciences field
Location & Eligibility
Where is the job
Pasig City, Philippines
On-site at the office
Who can apply
PH
About this job
- Who can apply
- Philippines
- Posted
- Today
Listing Details
- Posted
- November 4, 2026
- First seen
- November 4, 2026
- Last seen
- November 4, 2026
Posting Health
- Days active
- 0
- Repost count
- 1
- Trust Level
- 53%
- Scored at
- November 4, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
ClinChoice is a global full-service CRO that specializes in accelerating drug and device approvals across various healthcare sectors.
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