Empleos de junior clinical trial associate en Valencia

** Please submit your application and CV in English ** What You'll Do: * Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead. * Set goals, and timelines, provide oversight and positive leadership to foster motivation within the team to accomplish goals within defined timelines and with...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description The Senior Contract Associate is...

ICON Plc is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities, ensuring compliance with protocol, regulatory requirements and industry standards. You will lead monitoring tasks with technical depth, focusing on quality and continuous improvement.You will monitor sites, conduct visits, collaborate with...

ICON Plc is seeking a Senior Clinical Research Associate to work on a home-based basis in Spain. You will oversee clinical trial monitoring activities, ensuring compliance with protocols, regulatory requirements, and GCP standards while supporting site staff and cross-functional teams. The role emphasizes independent work, training of staff, and maintaining...

Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation?We are seeking a CRA II to manage investigative sites across Spain, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements.Key ResponsibilitiesConduct site qualification,...

Work ScheduleEnvironmental ConditionsJob DescriptionReady to take the next step in your CRA career?At CRG Thermo Fisher Scientific, we are offering an exciting opportunity to join a dedicated partnership with a leading global pharmaceutical company — giving you the chance to grow your career in a dynamic, client-dedicated environment.? Are you an Assistant...

What You'll Do: * Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead. * Set goals, and timelines, provide oversight and positive leadership to foster motivation within the team to accomplish goals within defined timelines and with high quality in the execution of assigned clinical...

Thermo Fisher Scientific is seeking a Senior Research Associate to lead de novo data collection projects across retrospective, prospective, and cross-sectional designs. You will draft protocols and reports, coordinate teams, and interact with sponsors and clinical sites under senior staff oversight.The role requires a PhD in epidemiology or MSc with 3-5...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThermo Fisher Scientific Inc. is a premier company that is dedicated to enabling our customers to make the world healthier, cleaner, and safer. We are a team of 100,000+ colleagues who share a common set of values - Integrity, Intensity, Innovation, and Involvement. Together, we work...

Senior Clinical Research AssociateAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that...

Premier Research is looking for a Senior Regulatory Submissions Lead to join our Regulatory Submissions and Contracts team.You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we...

Career Category Clinical Job Description What you will do In this role, the Clinical Scientist Associate Director supports the design, execution, and oversight of clinical trials and other late-phase global clinical studies. The role contributes to protocol development, study execution, medical monitoring support, and clinical data review, ensuring delivery...

Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to...

Precision for Medicine is seeking a Senior Clinical Research Associate in Spain to support a strategic sponsor in a fully home-based role. You will work within a quality-focused, collaborative environment and help ensure studies are conducted per protocol, ICH-GCP, and SOPs. You will monitor site performance, identify risks, train junior staff, and liaise...

Precision for Medicine seeks a Senior Clinical Research Associate to support a dedicated FSP partnership in Spain. This evergreen posting keeps a pipeline for future opportunities where CRAs monitor sites, ensure ICH-GCP compliance, and liaise with sponsors. Remote work in Spain is possible, with travel as needed. We value meticulous, proactive professionals...

Senior Clinical Research Associate - FREELANCE - 0.2 - 0.4 FTE Join ProPharma as a Freelance Senior Clinical Research Associate (SCAR) working 0.2–0.4 FTE in Spain. Responsibilities * Manage one existing site and set up/monitor three new sites for a study. * Conduct all types of monitoring: site initiation, interim, close‑out, co‑monitoring visits both...

Senior Feasibility Associate / Feasibility Manager Remote, Spain Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. Position Summary: The Senior Feasibility...

The Clinical Operations Manager is responsible for the day-to-day management of an assigned team of both permanent and contracted staff (e.g., Clinical Research Associates (CRA)/(cCRA)) and other Clinical Operations Support personnel) overseeing their performance and training, ensuring adequate monitoring and support team resources, allocating resources to...

## Associate II, TMF Operations - EMEA- Fixed term - RemoteApplyremote type: Remotelocations: Zagreb, Croatia: Barcelona, Spain: Virtual United Kingdom: Tbilsi, Georgia: Belgrade, Serbiatime type: Full timeposted on: Posted Todayjob requisition id: JR101863**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the...

Overview As a Project Director, you lead global oncology clinical trial programs, overseeing study portfolios and cross-functional teams to ensure on-time, within-scope delivery. You partner with clients to align on goals, drive process improvements, and maintain high-quality execution across studies. You shape trial strategy, risk management, and change...