Clinical Trial Management Expert

**Job Description**:Se nos conoce como Merck & Co., Inc., Kenilworth, Nueva Jersey, EE.UU., en Estados Unidos y Canadá, y como MSD en el resto del mundo.Durante más de un siglo hemos estado inventando para la vida, desarrollando fármacos y vacunas para muchas de las enfermedades más difíciles del mundo.Actualmente, nuestra empresa sigue estando a la...

**Job Description**:Se nos conoce como Merck & Co., Inc., Kenilworth, Nueva Jersey, EE. UU., en Estados Unidos y Canadá, y como MSD en el resto del mundo. Durante más de un siglo hemos estado inventando para la vida, desarrollando fármacos y vacunas para muchas de las enfermedades más difíciles del mundo. Actualmente, nuestra empresa sigue estando a la...

**Job Description**:Se nos conoce como Merck & Co., Inc., Kenilworth, Nueva Jersey, EE.UU., en Estados Unidos y Canadá, y como MSD en el resto del mundo.Durante más de un siglo hemos estado inventando para la vida, desarrollando fármacos y vacunas para muchas de las enfermedades más difíciles del mundo.Actualmente, nuestra empresa sigue estando a la...

**Job Description**:Se nos conoce como Merck & Co., Inc., Kenilworth, Nueva Jersey, EE. UU., en Estados Unidos y Canadá, y como MSD en el resto del mundo. Durante más de un siglo hemos estado inventando para la vida, desarrollando fármacos y vacunas para muchas de las enfermedades más difíciles del mundo. Actualmente, nuestra empresa sigue estando a la...

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...

Job SummaryThis role is responsible for overseeing the end-to-end performance and project management of assigned protocols in a country, ensuring compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards, and adverse event reporting requirements.About UsMsd is a leading healthcare company dedicated to improving lives...

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)...

¿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 crecimiento**Estas son algunas de las funciones que realizarás como practicante de Clinical Trial Operations**- Esta...

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...

**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...

**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...

The 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 members.Essential Functions:...

Job SummaryThe COL is responsible for the execution of Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies. This involves applying clinical research expertise, exceptional decision-making skills, and innovative approaches to problem-solving.Main Responsibilities:Oversee the delivery of Site Management project tasks,...

About the JobWe are seeking an experienced Clinical Data Science Project Lead to join our team in Mexico & Colombia. As a key member of the Early Phase Data Management department, you will play a crucial role in managing data management teams, studies, and programs. Your primary responsibility will be to oversee the entire life cycle of studies, from...

IQVIA is Seeking a Clinical Data Services Director:This exciting opportunity is for a seasoned professional to lead our Clinical Data Management (CDM) team. As a Clinical Data Services Director, you will be responsible for ensuring that all data management services meet the highest standards of quality, timeliness, and...

The 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 members. Essential Functions: ...

About the RoleThe RWE Clinical Operations Lead will lead the execution of Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies. This role involves developing and implementing strategies to ensure successful project outcomes.Key Responsibilities:Develop and execute project plans, ensuring timely and within-budget delivery...

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...

The Clinical Operations Director will lead the execution of Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies.Key Responsibilities:Oversee the delivery of Site Management project tasks and provide advice to achieve high performance and quality project deliverables.Ensure overall project efficiency and adherence to...

About VaxTRIALSVaxTRIALS is an Emmes Company that provides Clinical Study Services to customers across Latin America. As a full-service Contract Research Organization (CRO), we offer a diverse portfolio of services including study start-up, site management, data management, biostatistics, and regulatory affairs.We use Veeva Vault as our electronic Trial...