clinical trials

Cencora is seeking a Pharmacist Operating Assistant in Mexico to support the Depot Pharmacist and Auxiliary Pharmacist in depot tasks, ensuring proper reception, storage and shipment of materials.You will work with CTM-Star to handle inbound, outbound and return processes, coordinate shipments with Logistics and Clinical Trials Supply Chain Services, and...

At Johnson & Johnson, the largest healthcare company in the world, we come together with one purpose: to profoundly change the trajectory of health for humanity. Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for...

Worldwide Clinical Trials is seeking a Contract Manager to oversee contract development, budgeting and change orders with sponsors. You will draft, negotiate and finalize agreements, ensuring compliance with master agreements and internal policies.Collaborate with Legal, Global Proposal Development and Finance to secure approvals, update study budgets and...

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific timelines and enrollment goals.You will act as the main line of communication between Sponsor or CRO and the site, assist in scheduling and preparing for monitoring visits, track patient enrollment, maintain study...

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific timelines and enrollment goals.You will act as the main line of communication between Sponsor or CRO and the site, assist in scheduling and preparing for monitoring visits, track patient enrollment, maintain study...

Ceribell, Inc. in Sunnyvale, CA, is seeking a Director of Clinical Affairs to shape the evidence strategy and lead clinical trials for current and future products.You will partner with Regulatory, R&D, and Commercial teams to translate clinical data into market-ready plans and publications. You will oversee protocol design, data analysis, and regulatory...

Important: submit your CV in englishJob OverviewThe Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in SAS programming and familiarity with CDISC standards, particularly ADaM and SDTM models. Key responsibilities include...

Company DescriptionPSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...

Worldwide Clinical Trials is seeking a Contract Manager to oversee contract development, budgeting and change orders with sponsors. You will draft, negotiate and finalize agreements, ensuring compliance with master agreements and internal policies.Collaborate with Legal, Global Proposal Development and Finance to secure approvals, update study budgets and...

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within study-specific timelines and enrollment goals.You will act as the main line of communication between Sponsor or CRO and the site, assist in scheduling and preparing for monitoring visits, track patient enrollment, maintain study...

Ceribell, Inc. in Sunnyvale, CA, is seeking a Director of Clinical Affairs to shape the evidence strategy and lead clinical trials for current and future products.You will partner with Regulatory, R&D, and Commercial teams to translate clinical data into market-ready plans and publications. You will oversee protocol design, data analysis, and regulatory...

Syneos Health seeks a Project Data Manager to lead data management activities across clinical programs and coordinate a Data Management/Data Operations team. You will ensure milestones align with SOPs and interact with Clinical Monitoring, Project Management, and Finance. This role requires strong data management experience, project leadership, and CRO...

ICON plc is seeking a Laboratory Project Manager to design and oversee clinical trials, interpret complex data, and contribute to innovative therapies. The role involves managing multiple studies, representing ICON at sponsor meetings, and ensuring sponsor satisfaction. The ideal candidate has a scientific degree and 2+ years in clinical research or project...

Syneos Health seeks a Project Data Manager to lead data management activities across clinical programs and coordinate a Data Management/Data Operations team. You will ensure milestones align with SOPs and interact with Clinical Monitoring, Project Management, and Finance. This role requires strong data management experience, project leadership, and CRO...

ICON plc is seeking a Laboratory Project Manager to design and oversee clinical trials, interpret complex data, and contribute to innovative therapies. The role involves managing multiple studies, representing ICON at sponsor meetings, and ensuring sponsor satisfaction.The ideal candidate has a scientific degree and 2+ years in clinical research or project...

Worldwide Clinical Trials is seeking a Contract Manager in Mexico City to oversee contract development, amendments, and change orders with sponsors. You will draft budgets, scopes of work, and terms, lead negotiations, and ensure compliance with master agreements across global contracts.You will work with Legal, Global Proposal Development, and Finance to...

Worldwide Clinical Trials is seeking an RTSM Project Manager to lead RTSM initiatives across studies within a CRO environment. The role emphasizes coordinating cross-functional teams, maintaining project timelines, and ensuring high-quality RTSM deliverables while engaging sponsors and internal stakeholders.The candidate will bring 2+ years in RTSM and 1+...

Fortrea is seeking a regulatory affairs professional to support study maintenance and site startup activities, ensuring investigator and regulatory documents meet EC/IRB/Regulatory Authority timelines. With guidance from senior staff, you will develop awareness of applicable regulatory legislation and guidance in assigned countries.You will assist in...

Worldwide Clinical Trials in Mexico seeks a Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed accurately and on time. You will handle system access, maintain project documentation, assist with Investigator Site File shipments, and help keep trial master file versions up...

ICON plc is seeking an Associate Project Manager, Laboratory to lead and coordinate clinical trials within the Lab division in Mexico City. You will oversee multiple studies, liaise with sponsors, and ensure adherence to GCP standards while maintaining data integrity and timelines.Ideal candidates hold a science degree, have 2+ years in clinical research or...