Empleos de clinical data en San Jose

Job Overview:Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all DM activities (from study start-up to database lock) according to client quality expectations, within...

Job DescriptionActivities may include, but are not limited to: ·       Build, integrate, and maintain clinical databases and study systems, including transformations, edit checks, reporting, and user testing, while supporting governance of cross‑study programming environments.·       Design, develop, test, and maintain clinical technology...

Job DescriptionThe Associate Director, Study Data Services (M-track) leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners. Provide hands-on technical review, solutioning support, enforce SOPs/standards, manage...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Do you want to make a global impact on patient health? Do you thrive in a fast-paced environment that integrates scientific, clinical, and commercial domains through engineering and AI? Join Pfizer US Commercial AI Acceleration (AIA) team to leverage cutting-edge technology for critical business decisions and enhance customer experiences for colleagues,...

Vault RIM process and system is highly dependent on accurate & complete metadata at all levels and there is also ​an increasing amount of data that Health Authorities are requiring to be tracked and submitted.​The Regulatory Data Coordinator is responsible for driving key & critical activities within the Pfizer RIM system in support of enabling the...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure...

Job Overview:The Clinical Data Manager, Third-Party Data Acquisition (TPDA) will work within a sponsor-dedicated model, partnering closely with sponsor stakeholders, study teams, external data vendors, and cross-functional functions to support the acquisition, integration, and oversight of third-party clinical trial data.This role specializes in non-EDC...

The DCT Lead, Clinical Trial Configuration will work within a sponsor-dedicated model, partnering closely with sponsor stakeholders and cross-functional clinical study teams to support the implementation, delivery, and oversight of clinical technologies used across clinical trials.This role serves as a Clinical Technology Subject Matter Expert (SME) within...

The Senior Medical Coding Specialist will work within a sponsor-dedicated model, partnering closely with sponsor stakeholders and cross-functional clinical data management teams to provide medical coding expertise, oversight, and quality review across clinical development studies.This role serves as a Medical Coding Subject Matter Expert (SME) responsible...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global...

Senior Coding Specialist📍 Costa Rica ✅ Candidates must be based in Costa RicaAre you passionate about medical coding quality and clinical data integrity? We’re looking for a Senior Coding Specialist based in Costa Rica to support high‑quality, compliant clinical trial data across global studies.What you’ll doReview and ensure the quality and...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.As part of our global team,...

Clinical Data Specialist – Coordinator📍 Location: Costa Rica (candidates must be based in Costa Rica)🧬 Department: Clinical Data ManagementAdvance clinical research through data precisionWe are looking for a detail-oriented and collaborative Clinical Data Specialist – Coordinator to join our growing Clinical Data Management team.In this role, you...

OBJECTIVEConduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to Patient Safety. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of noncompliance.Ensure and monitor compliance...