Marc Wilson Lim

Associate Principal Regulatory Writer @Certara

Durham, NC, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Apr 2025 — Present

Associate Principal Regulatory Writer @Certara

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Authored documents per client specifications and guidance documents. Document types include clinical pharmacology/pharmacometrics (PK NCA, PopPK, and ER analyses) and clinical study (CSR) reports; investigator\'s brochure (IB); clinical study protocol; new drug application (NDA) and biologics license application (BLA) eCTD modules 2.7.1 (SBS) and 2.7.2 (SCP); integrated summary of immunogenicity (ISI); and briefing documents.• Served as client advisor, working with all parties to develop strategies for organizing and preparing regulatory documents.• Ushered documents through the review process, conducted comment resolution meetings, and led project teams to consensus.

EDUCATION

N/A

University of the Philippines

Bachelor's Degree, Industrial Pharmacy

SKILLS

HealthcarePharmaceutical ResearchPharmaceutical SciencesClinical TrialsDrug DevelopmentPharmaceutical IndustryDrug SafetyGlpAnalytical Method ValidationPharmaceutical ManufacturingClinical ResearchClinical PharmacologyQuality AssuranceTeachingPharmacovigilanceQuality ControlPharmacologyGmpRegulatory Affairs

ABOUT MARC WILSON LIM

Pharmacist with close to a decade of combined pharmaceutical industry experience across the areas of regulatory writing and pharmacovigilance.

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