Start-up Specialist

Main Requirements - 3+ years of industry related experience, including handling of trial start-up activities coordination of trial start-up activities and Health Authority / Ethic Committee submissions and contract negotiation Must Have - Minimum qualifications posted above; - Thorough understanding of GCP, ICH Guidelines and Country regulatory...

Subject Matter Expert on Clinical Trials / Clinical Research Legislation **Requirements**: - Support CH / Country Lead Monitors in the planning of the Clinical Trials submissions /regulatory strategy **Minimum Previous Experience**: - ** EU CTD submissions to CEIC - more than 2/3 years of experience**: - EU CTR knowledge and submission preparation is...

A global clinical research organization is seeking a Regulatory Affairs Study Start-Up Specialist II to manage regulatory submissions and provide support for clinical studies. The ideal candidate should have at least 3 years of experience in regulatory affairs within the CRO or pharmaceutical industries, and be fluent in English. This position offers...

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...

The surgical robotics utilization team manages all aspects of system installation, start-up, customer training, account analysis, drive and optimize the robotic program. Placement of a HUGO surgical robot in the hospital requires full-time support for an account specific period to ensure successful integration into the hospital’s service lines. The...

Labcorp Drug Development As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. **A Day in the Life **:The surgical robotics utilization team manages all aspects of system installation, start-up,...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life The surgical robotics utilization team manages all aspects of system installation, start-up,...

Regulatory and Start Up Manager, IQVIA MedTech, Portugal page is loaded## Regulatory and Start Up Manager, IQVIA MedTech, Portugallocations: Lisbon, Portugaltime type: Full timeposted on: Posted Todayjob requisition id: R1512190**Job Overview**Direct and manage the delivery of all required site activation, maintenance and regulatory activities for...

**Remote Backoffice Specialist (Dutch Market) - Full-time | Based in Portugal** **Backoffice Specialist (Nederlandstalige markt) op afstand - Voltijds | Vanuit Portugal** We are hiring native/fluent **Dutch speakers with good English (B2+)** for **three remote backoffice roles** supporting a leading global technology company. Wij zijn op zoek naar...