clinical trials

Our client, a prominent recruitment consultancy, is seeking an experienced and strategic Talent Acquisition Lead to join their fully remote team. This pivotal role will be instrumental in shaping and executing innovative talent acquisition strategies that meet the evolving needs of our diverse clientele. You will lead the end-to-end recruitment process,...

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...

Job 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 developing and validating complex data...

Worldwide Clinical Trials is seeking a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks are performed timely and accurately.You will manage system access for project staff, maintain document control, assist with preparation and shipment of trial documentation, keep trial...

Job Overview The 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 developing and validating complex data...

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...

Signant Health seeks an experienced Project Manager to drive end-to-end delivery of advisory, eCOA, and RTSM projects across client programs. You will manage budgets, timelines, resources, and quality while ensuring regulatory and contractual compliance in a highly regulated environment.As a proactive leader, you will coordinate cross-functional teams,...

ICON is a global healthcare intelligence and clinical research organisation dedicated to accelerating access to new medicines. The role supports investigator sites with administrative and operational activities to ensure trials run smoothly, in compliance with ICH/GCP.Based in Mexico City, this hybrid position involves coordinating site activation tasks,...

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...

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...

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...

ICON is a global healthcare intelligence and clinical research organisation dedicated to accelerating access to new medicines. The role supports investigator sites with administrative and operational activities to ensure trials run smoothly, in compliance with ICH/GCP.Based in Mexico City, this hybrid position involves coordinating site activation tasks,...

Job 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 developing and validating complex data...

Cencora seeks a Pharmacy Operations Assistant to support the Depot Pharmacist and Auxiliary Pharmacist, handling inbound, outbound and return processes in CTM-Star and ensuring compliance with SOPs for reception, storage and shipment of materials.You will coordinate shipments between Logistics areas and the Clinical Trials Supply Chain Service Division,...

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...

Signant Health seeks an experienced Project Manager to drive end-to-end delivery of advisory, eCOA, and RTSM projects across client programs. You will manage budgets, timelines, resources, and quality while ensuring regulatory and contractual compliance in a highly regulated environment.As a proactive leader, you will coordinate cross-functional teams,...

Signant Health seeks an experienced Project Manager to drive end-to-end delivery of advisory, eCOA, and RTSM projects across client programs. You will manage budgets, timelines, resources, and quality while ensuring regulatory and contractual compliance in a highly regulated environment. As a proactive leader, you will coordinate cross-functional teams,...

Syneos Health offers an ideal opportunity for a Project Associate or CTA/Project Specialist to support clinical trial management. The role emphasizes coordinating tasks, maintaining timelines and budgets, and collaborating with cross-functional teams to deliver high-quality studies.The position requires a life sciences background, strong organizational and...

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...

IQVIA is seeking a Project Manager to oversee small to mid-size Connected Devices projects across clinical trial phases. You will coordinate with senior project leadership to ensure deliverables meet sponsor expectations, on time and within budget.Your role focuses on leading cross-functional teams, managing risks, and maintaining strong client relationships...