Open to opportunities

Maureen Lemoha

@maureenlemoha

Drug safety and pharmacovigilance professional delivering accurate ICSR case processing and patient-centered clinical support.

United States

Message

What I'm looking for

I’m looking for a drug safety/pharmacovigilance role where I can own ICSR case processing, coding, and quality review, collaborate across medical and regulatory teams, and deliver timely, compliant safety reporting with strong SOP and GxP standards.

I’m a highly organized, detail-oriented medical professional with extensive healthcare and clinical research experience, focused on safe, patient-centered care. I consistently establish rapport, communicate clearly across teams, and adapt quickly to evolving clinical needs.

In drug safety and pharmacovigilance, I’ve supported end-to-end case processing in safety databases and ensured timely, compliant reporting of AEs/SAEs and follow-up information. I’m skilled in medical coding with MedDRA and WHO drug dictionary, performed quality review for AEs/SAEs/SUSARs, and used tools such as Argus Safety and ARISg while collaborating regularly with CRO and cross-functional partners to resolve safety-related issues.

Experience

Work history, roles, and key accomplishments

Pharmacovigilance Specialist

MediPharm Solutions

Mar 2024 - Mar 2025 (1 year)

Collaborated with medical, clinical, and regulatory teams to assess case reportability and process serious adverse events in line with sponsor SOPs. Coded AEs using MedDRA/WHO DD, completed case management (triage, duplicate checks, narratives, follow-ups, QC), and submitted ICSRs to regulatory authorities within required timelines.

Pharmacovigilance Medical Coding WHO DD ICSR Case Processing SAE SUSAR Safety QC Review Regulatory Reporting Case Triage And Duplicate Checks