Global Clinical Trials Lead

About the RoleThe Clinical Operations Lead at IQVIA is accountable for leading the Clinical Data Management (CDM) team, ensuring high-quality, timely, and cost-effective data management services for projects.You will be responsible for providing expertise and vision in project planning, execution, and close-out, while ensuring compliance with Good Clinical...

**Practicante** **Clinical Trial Operations** - **Finanzas**¿Estás listo para poner en práctica tus conocimientos, aprender e impactar en millones de vidas?Si es así, esta es la oportunidad perfecta para que hagas parte de una empresa que le apuesta a la innovación, la experimentación y el crecimientoEl practicante de Global Clinical Trial Operations...

About the RoleWe are seeking an experienced Associate Director of Data Management to join our team at MSD. In this role, you will be responsible for leading Senior clinical data managers and Clinical Data Managers in operations tasks within a Data Management Center. The successful candidate will have a strong background in Clinical Trials and experience in...

The Clinical Research Manager is a key member of the MSD team, responsible for the end-to-end performance and project management of assigned protocols. This role requires strong leadership skills, excellent communication, and a proven track record of delivering results in a fast-paced environment.About the Role:This position will be accountable for the...

Merck Gruppe - MSD Sharp & Dohme is seeking a highly skilled Clinical Safety Specialist to support safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development.The ideal candidate will assist the protocol lead in safety reporting activities for...

Las mejores invenciones no se llevarían al mercado sin la gestión de proyectos y el apoyo administrativo adecuados.Nuestros equipos administrativos, entrelazados en cada parte de la organización, aseguran que nuestros conceptos se hagan realidad.Como Aprendiz SENA prestarás apoyo al área de Global Clinical Trials Operation en diferentes labores que van...

About UsICON plc is a global leader in healthcare intelligence and clinical research, driven by a passion for innovation and excellence. We create an inclusive environment that fosters collaboration and growth, empowering our employees to reach their full potential.We prioritize continuous learning and professional development, recognizing that every...

About the RoleWe are seeking a highly experienced Clinical Data Governance Specialist to join our Real World Evidence team. As a key member of the team, you will be responsible for leading the Clinical Data Management (CDM) team, providing expertise and vision in project planning, execution, and close-out.ResponsibilitiesOversee the delivery of high-quality...

Job SummaryWe are looking for a highly skilled Clinical Support Manager to join our team in Colombia. As a key member of our Medical Affairs team, you will play a critical role in providing scientific information and support to external stakeholders, including healthcare professionals and researchers. Your expertise will be instrumental in delivering...

Key ResponsibilitiesThis Principal Clinical Data Science Lead will manage fast-moving early phase studies or programs of studies to ensure project objectives are met within budget, to agreed timelines, and to a high level of quality. You'll work closely with Clinical Operations, Biostatistics, SAS Programming, Medical Writing, and Quality Assurance to ensure...

At our global company, we value dedication and hard work. As a Clinical Research Site Coordinator, you will have the opportunity to advance your career in clinical research while making a difference in the lives of others.ResponsibilitiesYour key responsibilities will include:Being the main point of contact between site personnel and CRA involved in the...

**Key Responsibilities**Manage data management teams, studies, and programs of studies.Provide planning estimates for project scope, schedule, and resource requirements.Work with Clinical Operations, Biostatistics, SAS Programming, Medical Writing, and Quality Assurance to ensure data collected during trials is managed according to corporate standards and...

Job OverviewThe Global Data Management Lead will play a critical role in driving the strategy and direction of our global data management function. You will lead a team of senior clinical data managers and clinical data managers, providing guidance and support to ensure the successful delivery of projects and initiatives. Key responsibilities include:Leading...

As a member of MSD’s clinical research team, you will play a critical role in ensuring the successful execution of clinical trials. The Clinical Research Manager will be responsible for managing the day-to-day activities of assigned protocols, including project planning, site management, and quality control.Key Responsibilities:Main Point of Contact (POC)...

Maintaining the highest level of quality and integrity in clinical trials requires a Pharmaceutical Clinical Safety Professional with expertise in safety reporting.MERCK Gruppe - MSD Sharp & Dohme is searching for an experienced professional to support safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational...

Sr. Scientist, Drug Safety- Bogotá, Bogota D.C. Merck Gruppe - MSD Sharp & Dohme 12.03.2025Job DescriptionClinical Safety and Risk Management Associate: In conjunction with the CSRM team, works to expand and apply clinical, pharmacological, and epidemiologic knowledge and information.Scientist, Drug Safety (Término Fijo)- Bogotá, Bogota D.C. Merck Gruppe...

As a Clinical Excellence Professional at Novartis, you will contribute to the success of our global clinical trials by ensuring compliance with industry standards, country regulations, and internal policies. Your role will involve providing oversight of vendors and third-party services involved in the planning and execution of projects. You will also act as...

Safety Scientist Position available at MERCK Gruppe - MSD Sharp & Dohme to support safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development.The successful candidate will have prior experience in patient care settings, drug safety and...

This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. The CRM could be responsible for a particular study for...

Clinical Operations LeadThe COL leads the execution of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision-making skills, and innovative approaches to problem solving. Proactively set project goals and tangible expectations for SPS project team...