Clinical Trial Manager

IQVIA's cFSP team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward. Great opportunity to shape local component of global study (UK remit / 2 studies across 8-10 sites / phase I-III). Sponsor dedicated to one of the world's largest pharmaceutical companies. Fully remote with minimal travel. RESPONSIBILITIES Partner...

Job Overview Perform 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. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

IQVIA’s cFSP team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward. Great opportunity to shape local component of global study (UK remit / 2 studies across 8-10 sites / phase I-III). Sponsor dedicated to one of the world’s largest pharmaceutical companies. Fully remote with minimal travel. RESPONSIBILITIES ...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to administratively and...

Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA page is loaded Regulatory Manager, Clinical Trials Regulatory Management- Home-based, EMEA Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria time type Full time posted on Posted 7 Days Ago job requisition id...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

**Salary**:£13.77 per hour PAYE - **REF Number**:00056344 - **Consultant**:Lucy Pinnick - **Contact**:01246 457725 - **Date Published**:23.11.2023 - **Sector**:Clinical Research - **Location**:Reading, South West - **Discipline**:Clinical Operations CK Group are recruiting for an Clinical Study Assistant to join a company in the Clinical Research industry...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complex Ability to administratively and technically/scientifically review core scientific documentation...

As a Director within the Strategic Site Solutions team, you will be responsible for developing and delivering site-based network strategies to deliver growth, differentiation, and superior performance across the IQVIA human data science business. The role is focused on growing and maintaining two regional site networks, a Cell & Gene Therapy site network and...

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardWhy IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that support flexible...

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardWhy IQVIA?Growth potential - clear pathways to success for those who want to grow with usProfessional development - resources that promote your career growth and programs to help you build knowledge and gain skillsWork-life balance - leaders that support flexible...

Vendor Program Manager Key accountabilities  Provides vendor oversight and management at a trial level to ensure all vendors deliverables are done timely & good quality Coordinates vendor deliverables across VSE during study start-up Covers all vendor activities after study start-up and all categories not covered by VSEs: Drives and monitors...

Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! Why IQVIA? Growth potential - clear pathways to success for those who want to grow with us Professional development - resources that promote your career growth and programs to help you build knowledge and gain skills Work-life balance - leaders that...

IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare...

About us: **About the role**: As the Ostomy Clinical Resource Specialist based in Ohio, you will play a pivotal role in driving profitable business results through the execution of Convatec's current business strategies. Your key responsibility will be to foster high-level customer relationships by providing essential clinical support to our dynamic sales...

**Clinical Sales Specialist - Wound Closure - UK** As part of a team expansion project across the EU, IQVIA is recruiting for several field-based sales positions in France, Netherlands, Italy, Germany, and the UK on behalf of our client - a highly respected global company renowned for its innovation and success within pharmaceutical, consumer health and...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UKJoin us on our exciting journeyRemote/Hybrid/Office based working options.Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forwardAs Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that...

Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UKJoin us on our exciting journey!Remote/Hybrid/Office based working options.Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!As Clinical Research Associate you will be responsible perform monitoring and site management work to ensure that...

Role Overview: The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks, IQVIA is able to relieve the...