Empleos de compliance associate ii en Valencia

Worldwide Clinical Trials is seeking an Associate II, TMF Operations to join a global TMF team. You will review, process, and quality-check TMF documents, ensuring completeness and regulatory compliance across complex studies and sponsor portfolios. You will collaborate with global project teams, RMC leads, and internal groups to identify TMF trends, resolve...

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials , we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around...

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the...

## Associate II, TMF Operations (Europe/LATAM)Apply: Remote: England, United Kingdom: Valencia, Spain: Virtual Mexico: Virtual Czechia: Virtual Hungary: Full time: Posted Today: JR Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives through...

## Associate II, TMF Operations (Europe/LATAM)Apply: Remote: England, United Kingdom: Valencia, Spain: Virtual Mexico: Virtual Czechia: Virtual Hungary: Full time: Posted Today: JR Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives through...

Imagine how your ideas and expertise can change a patient’s life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You’ll bring your passion for problem solving and partner with various teams to influence decision‑making...

Worldwide Clinical Trials is seeking an Associate II, TMF Operations for a remote European-based role. You will review, process, and quality-check TMF documentation across complex studies, ensuring ALCOA principles and ICH GCP standards are met. You will collaborate with global teams, prepare QC checklists, and maintain study documentation while supporting...

Edwards Lifesciences in Valencia, Spain, seeks a Quality Specialist to support medical device complaint handling and regulatory reporting. You will investigate complaints, evaluate events, and manage customer expectations throughout the resolution process.Strong documentation and communication skills are essential. Required are a related bachelor's degree...

## Associate II, TMF Operations (Europe/LATAM)Apply: Remote: England, United Kingdom: Valencia, Spain: Virtual Mexico: Virtual Czechia: Virtual Hungary: Full time: Posted Today: JR Join a global Contract Resource Organization (CRO) where innovation meets purpose. At **Worldwide Clinical Trials**, we're driven by a shared commitment to improving lives through...

Edwards Lifesciences in Valencia, Spain, seeks a Quality Specialist to support medical device complaint handling and regulatory reporting. Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura. You will investigate complaints, evaluate events, and manage customer expectations...

Worldwide Clinical Trials is seeking an Associate II, TMF Operations for a remote European-based role.Para presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes.You will review, process, and quality-check TMF documentation across complex studies, ensuring ALCOA principles and ICH...

PSI CRO in Spain is seeking a Clinical Research Associate II to lead on-site monitoring across Phase II/III studies, ensuring data quality and regulatory compliance. You will build strong relationships with sites and investigators, manage communications with cross-functional teams, and support feasibility studies and regulatory submissions.The role requires...

About AlantraAlantra is an independent global financial services firm that provides investment banking and asset management services to midmarket companies, families, and investors. The Group has over 500 professionals in Europe, the U.S., Latin America, Asia, and the Middle East.In Investment Banking, Alantra has completed over 1,000 transactions in the...

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Quality Engineer II — Medical Device (Onsite — Valencia, CA) Possible Contract ExtensionValencia, United States | Posted on 04/28/2026From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues.We collaborate with our partners by providing technical...

Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU 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,...

Amadeus Hospitality in Valencia (FWK) is seeking a Data Management & Governance Associate to support governance policies, metadata management, and compliance across business domains. The role emphasizes accurate, secure data and collaboration with Legal, Security, and Technology teams.You will help maintain Collibra artifacts, data inventories, data lineage,...

Quality Engineer II — Medical Device (Onsite — Valencia, CA) Possible Contract ExtensionValencia, United States | Posted on 04/28/2026From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues.We collaborate with our partners by providing technical...

Medical Data Specialist II — Medical Device (Hybrid — Valencia, CA) Contract Valencia, United States | Posted on 10/21/2025 From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues.We collaborate with our partners by providing technical expertise in...

Join us in redefining what it means to work for a CRO.When you work at Rho, it's more than just a job—you become part of the Rho Factor. We're a proud bunch of science nerds who love tackling big challenges together. We're not your typical CRO, and we're not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at...