Senior Clinical Trial Manager - Stockholm

The Manager, Trial Delivery Management (TDM) is responsible for the execution of study-level activities and overseeing local operational delivery at a country or regional level. · ...

The Senior Clinical Trial Manager is responsible for providing end-to-end operational oversight of an oncology clinical trial across multiple European countries.Provide operational oversight and execution of a global Phase 2 oncology clinical trial across multiple European countr ...

We are now looking for a Trials Coordinator who will play a key role in delivering smooth and professional device trials to customers. · ...

We are now looking for a Trials Coordinator who will play a key role in delivering smooth and professional device trials to customers. · Coordinating and scheduling device trials in collaboration with Sales, Solutions Consultants, and Logistics teams · ...

Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors studies or multi-protocol programs as determined by the Sponsor's requirements. · Prepare negotiate and finalize clinical trial agreements and an ...

The Clinical Trial Associate supports clinical study teams by coordinating operational activities and ensuring accurate setup, · maintenance, and closure of the Study Master File in compliance with GCP, · SOPs, · and regulatory requirements. · This role is part of our SRS team, · ...

Developthe globalcontractingstrategyandsupportthedeliveryofallrequiredstart-upcontractingactivitiesforselctedsponsors,studiesormultiproto-gramasdeterminedbythesponsor'srequirements. · ...

The Clinical Trial Associate supports clinical study teams by coordinating operational activities and ensuring accurate setup, maintenance, and closure of the Study Master File in compliance with GCP, SOPs, and regulatory requirements. · ...

The Clinical Trial Associate (CTA) supports clinical study teams by coordinating operational activities and ensuring accurate setup, · maintenance, and closure of the Study Master File in compliance with GCP,v SOPs,and regulatory requirements. · As part of our SRS team,you will w ...

We are seeking a project manager with documented experience in regulatory processes for medical devices, with a particular focus on software as a medical device (SaMD). The position entails primary responsibility for leading ClinAI Prostate – an AI-based analysis tool for digital ...

The IQVIA Dermatology Center of Excellence is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our Dermatology portfolio and advance this dynamic and rapidly expanding area of clinical development. · ...

Clinical Research Nurse to support a clinical research site in Stockholm. Part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. · Maintaining and updating study documentation, including protocols, case repo ...

+Job summary · The IQVIA CNS Center of Excellence is looking for a Board-Certified psychiatrist to join our team as a Medical Strategy Lead. · +ResponsibilitiesAccountable and responsible for creating innovative delivery strategies and solutions for CNS pre-approval clinical tria ...

The Clinical Expert/Clinical Study Physician will provide medical leadership and oversight for clinical trials in patients primarily with a central nervous system (CNS) disorder. · Ensure high quality strategic and operational leadership and expert input to assigned clinical deve ...

The IQVIA Cardiovascular Center of Excellence is looking for a Board-Certified cardiologist to join our team as a Medical Strategy Lead. · Accountable for creating innovative, evidence-based delivery strategies and solutions for Cardiovascular pre-approval clinical trials. · In p ...

Clinical Research Nurse to support a clinical research site in Stockholm. · ...

The Clinical Expert/Clinical Study Physician will provide medical leadership and oversight for clinical trials in patients primarily with a central nervous system (CNS) disorder. · Provide day-to-day medical oversight of the assigned clinical studies. · Review and adjudicate adve ...

This job involves performing monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · ...

We are recruiting on behalf of Valu8, a data and analytics platform built for Private Equity, M&A, · and corporate strategy teams. · ...

The Clinical Monitoring CRA I will oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location. · This includes conducting remote monitoring of trial sites to verify compliance with regulatory requirements and clinica ...