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Job Description The Senior Specialist, External Data Manager leads trial-level external data strategy and delivery studies. The role owns transfer-spec development, monitors transfers through conduct and lock, drives defect triage and resolution, ensures regulatory/SOP (Standard Operating Procedure) compliance and data readiness, and mentors junior analysts...

Job Description The Specialist, External Data Manager (EDM) supports teams in execution of trial-level external-data activities, authoring and maintaining transfer specifications and coordinating with service providers/IT for accurate ingestion. The role performs completeness, reconciliation, and traceability checks, applies standards and controlled...

Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy...

Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within Global Clinical Trial Operations (GCTO) creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws...

Merck & Co., Inc. in Rahway, NJ, USA seeks an experienced Clinical and Regulatory Medical Writer to lead preparation of regulatory documents and public-facing materials, ensuring accuracy, regulatory compliance, and clear communication. You will collaborate with cross-functional teams, apply health-literacy principles, and drive process improvements while...

Job Description The Specialist, External Data Manager (EDM) supports teams in execution of trial-level external-data activities, authoring and maintaining transfer specifications and coordinating with service providers/IT for accurate ingestion. The role performs completeness, reconciliation, and traceability checks, applies standards and controlled...

Job Description The Senior Specialist, External Data Manager leads trial-level external data strategy and delivery studies. The role owns transfer-spec development, monitors transfers through conduct and lock, drives defect triage and resolution, ensures regulatory/SOP (Standard Operating Procedure) compliance and data readiness, and mentors' junior analysts...

Propósito del Rol Buscamos un profesional apasionado por transformar el acceso a la salud y generar impacto sostenible en los resultados de los pacientes. Como Territorial Market Access Specialist, será responsable de diseñar e implementar, junto con EPS, IPS, Secretarías de Salud y demás actores del ecosistema, soluciones innovadoras que faciliten el...

Job Description Propósito del Rol Buscamos un profesional apasionado por transformar el acceso a la salud y generar impacto sostenible en los resultados de los pacientes. Como Territorial Market Access Specialist, será responsable de diseñar e implementar, junto con EPS, IPS, Secretarías de Salud y demás actores del ecosistema, soluciones innovadoras...

Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy...

Job Description The Clinical and Regulatory Strategic Communications department within Global Clinical Trial Operations (GCTO) creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while...

Job Description Propósito del Rol: Buscamos un profesional apasionado por transformar el acceso a la salud y generar impacto sostenible en los resultados de los pacientes. Como Territorial Market Access Specialist, será responsable de diseñar e implementar, junto con EPS, IPS, Secretarías de Salud y demás actores del ecosistema, soluciones innovadoras...

Job Description The Associate Director, CDM (Clinical Data Management) Geography Lead oversees day-to-day data-management operations and resources within the assigned geography. The role ensures operational efficiency, compliance, and quality delivery, supports regional strategy and resourcing, and partners with other leaders to promote consistent practices...

Job Description Demonstrates independence in preparing clinical regulatory (e.g., protocols, clinical study reports, participant narratives, investigator’s brochures) and/or public‑facing (e.g., informed consent forms, clinical trial registration and results postings, plain language summaries) documents per company and evolving regulatory requirements. ...

Job Description The Clinical and Regulatory Strategic Communications department within Global Clinical Trial Operations (GCTO) creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while...

Gerente de Estrategia de Acceso y Valor Propósito del cargo Liderar el diseño y desarrollo de estrategias de acceso y propuestas de valor para productos estratégicos y nuevos lanzamientos de la compañia , asegurando la incorporación sostenible de innovaciones al sistema de salud colombiano mediante la integración de evidencia clínica, económica y de...

Job Description The Senior Director, Clinical Data Management Therapeutic Area (TA) Lead, Hematology provides strategic and operational oversight of data management delivery across the assigned therapeutic area(s). The role leads portfolio planning, resource and performance management, and cross-functional alignment to ensure execution against GDMS and...

Job Description The Senior Specialist, External Data Manager leads trial-level external data strategy and delivery studies. The role owns transfer-spec development, monitors transfers through conduct and lock, drives defect triage and resolution, ensures regulatory/SOP (Standard Operating Procedure) compliance and data readiness, and mentors' junior...

Merck & Co., Inc. is seeking a Senior Medical Writer to develop, author, and lead the review of clinical, regulatory, and public-facing documents across multiple programs and therapeutic areas. The role requires collaboration with cross-functional teams, strong data interpretation, and leadership in a fast-paced, compliant environment. Hybrid work...

## Associate Dir. FA Geo Lead, Colombia, GDMS CDMApply: Hybrid: COL - Cundinamarca - Bogotá (Colpatria): Full time: Posted Today: End Date: October 29, 2026 (7 days left to apply): R Job DescriptionThe Associate Director, CDM (Clinical Data Management) Geography Lead oversees day-to-day data-management operations and resources within the assigned geography....