Study Start Up Manager-spain Wide-cro

The Study Start-Up CRA is accountable for site selections as well as study-specific start-up activities and deliverables of assigned sites for Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive site preparation and early identification of real site...

The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and collaborates with cross-functional teams to meet study timelines and client expectations. The ideal candidate will bring strategic...

Study Start Up Associate II - ICF ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development Study Start Up Associate (Informed Consent) We are looking for...

If you want to be part of a leading CRO and transform scientific discoveries into new treatments, thenParexel FSPchallenges you to live up to your potential by joining us atSSU Specialist Senior, home-based and sponsor dedicated, inSpain.The Senior Study Start-up Specialist is responsible for quality deliverables at the country level; follows project...

Manager, Study Start Up - Office Based - Madrid - Spain At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Associate Study Start-Up Manager IQVIA Biotech Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions: - Oversee the execution of Site Activation...

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Global Start-Up Assistant to join our A-team! The Global Start-up Assistant (GSUA) provides administrative support to all...

What You'll Do:Regulatory Submission ManagementPrepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS.Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions.Prepare and QC Clinical Trial Application...

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. Conducting operations in...