Regulatory & Clinical Research Coordinator (M/F)

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. **Join Our Team as a** **Senior Clinical Research...

EPM Scientific are currently partnered with a Mid-Sized CRO running a global project in Oncology. They are urgently seeking a Freelance Clinical Research Associate (CRA) to support their expanding clinical operations team. See a short summary below: **Contract Conditions**: - Start date: ASAP - Location: Portugal, Remote - Contract Type: Freelance /...

**CATO SMS and Pharm-Olam, LLC have merged to form Allucent!** **Allucent **is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical...

Join us in our exciting journey!! As an experienced Clinical Research Associate, you could be looking to broaden your therapeutic, geographic or study exposure. Or perhaps you are looking a future beyond monitoring with our selection of development opportunities. At IQVIA, you’ll have training and development to plan and progress your career in the...

Regulatory Affairs Study Start Up Specialist II (RASSU) Join to apply for the Regulatory Affairs Study Start‑Up Specialist II (RASSU) role at CTI Clinical Trial and Consulting Services. Responsibilities - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical...

Clinical Trial Administrator, Single Sponsor dedicated Job Overview: CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up...

Global Clinical Operations (GCO) Position Title: CLINICAL RESEARCH MANAGER (Functional Manager II) **Position Summary**: The Functional Manager II (FM II) is accountable for strategic and operational management and successful country execution of all phases of clinical trials within assigned therapeutic area(s) or specific role(s), including resource...

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our...

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our...