Clinical Operations team . At least 2-3 years of individual clinical trial monitoring experience; oncology, or other complex study monitoring is an advantage. High level of knowledge of ICH GCP Guidel...

Serving as a field resource for The Medical Affairs Company (TMAC), will represent the Company’s Respiratory Clinical Development program. The CTL will work full time to educate, analyze, and resolve ...

Připojte se k přední globální společnosti a podílejte se na vedení klinických studií, které posouvají hranice medicíny.Pokud máte alespoň 2 roky zkušeností v klinickém výzkumu a chcete pracovat v dyna...

Minimum of 1-2 years of medical equipment sales/clinical experience or minimum of 1-3 years in an operating room (as nurse, or product specialist, or clinical specialist, etc. Clinical Sales Represent...

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular t...

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular t...

Previous experience of leading studies as a Statistician within clinical research. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership wi...

We are Worldwide Clinical Trials, and we are a global team of almost 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best ...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular t...

The Clinical Supply Chain Manager is responsible for managing the strategic planning and execution of a program of assigned clinical supply chain projects. Interpret clinical trial protocols to create...

Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Experienced in the conduct of CSR/DM/BIOS clinical trial audits. IQVIA i...

In this role, you will… Drive growth and build clinical confidence of customers through education on Align’s clinical protocols and ClinCheck software program as well as clinical troubleshooting Provi...

CLINICAL TRIAL EXECUTION – PRECLINICAL, CLINICAL TRIALS FOR IN-HOUSE and CO-DEVELOPMENT PROJECTS. Clinical / preclinical program planning and Study Execution for in-house developed products, co-develo...

QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular t...

Senior Clinical Research Associate. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good knowledge of clinical research regulatory requirements.

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that a...

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.