Senior Associate, Medical Writing (MD)

ClinChoice; Pasig; Sur place; PHP 480 000 - 720 000; Plein temps

Résumé du poste

ClinChoice seeks a medical writer to support regulatory submissions and safety reporting, including CERs, SSCPs, PSURs, PMA/HDE IDE, and HEMA research. Role adapts to project needs and involves peer-review support to ensure timely, compliant delivery.

The position requires 1–3 years in medical writing, strong English, and excellent time management with minimal supervision. Adherence to QMS/ISMS/PIMS and data confidentiality is essential.

Qualifications

• At least 1-3 years of experience in medical writing, or any related field as applicable.
• Proficient in time management and can work with minimal supervision.
• Proficiency in oral and written English language.

Responsabilités

• Performs tasks according to the assigned medical writing activities including systematic literature reviews primarily for the generation of CERs, SSCPs, SOA, PMS including PSURs and PMA FDA Reports, HDE, IDE Reports, and HEMA research.
• Supports review of work done by peer teammates, on need basis.
• Alerts and escalates to senior members as required when project deliverables risk delay.
• 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.

Connaissances

Medical writing

Formation

Bachelor's degree in life sciences

Outils

MS Office

Description du poste

• 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

ROLE REQUIREMENTS:

• 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).

EDUCATIONAL QUALIFICATIONS:

• Minimum bachelor's degree in any life sciences field