Clinical Study Supervisor

Job SummaryWe are seeking a highly experienced and skilled Senior Director, Clinical Research Scientist to join our team at Advanced Clinical. This is a key leadership role that will be responsible for collaborating with physicians in Clinical Development to deliver clinical research support for assigned programs.Key ResponsibilitiesProtocol...

Job SummaryWe are seeking a highly experienced and skilled Senior Director, Clinical Research Scientist to join our team at Advanced Clinical. This is a key leadership role that will be responsible for collaborating with physicians in Clinical Development to deliver clinical research support for assigned programs.Key ResponsibilitiesProtocol...

Position OverviewProclinical Staffing is seeking a committed and detail-oriented Clinical Study Project Coordinator. This role operates in a hybrid model, necessitating in-office presence three days a week. The ideal candidate will assist the Clinical Study Lead in managing various aspects of clinical trial execution. This encompasses both studies conducted...

Position OverviewProclinical Staffing is seeking a committed and detail-oriented Clinical Study Project Coordinator. This role operates in a hybrid model, necessitating in-office presence three days a week. The ideal candidate will assist the Clinical Study Lead in managing various aspects of clinical trial execution. This encompasses both studies conducted...

Job SummaryVenn Life Sciences is seeking a highly skilled Study Physician to join our team in London. As a Study Physician, you will play a critical role in the success of our clinical trials, working closely with our research team to ensure the smooth execution of studies.Main ResponsibilitiesPerform clinical procedures as required within protocol, and...

Job SummaryVenn Life Sciences is seeking a highly skilled Study Physician to join our team in London. As a Study Physician, you will play a critical role in the success of our clinical trials, working closely with our research team to ensure the smooth execution of studies.Main ResponsibilitiesPerform clinical procedures as required within protocol, and...

Job DescriptionJob SummaryThe Global Medical Affairs team at the Healthcare Businesswomen's Association plays a critical role in shaping the medical strategy for our organization. As a Clinical Studies Director, you will be responsible for leading the development and execution of medical affairs strategies for our priority programs. This includes developing...

Job DescriptionJob SummaryThe Global Medical Affairs team at the Healthcare Businesswomen's Association plays a critical role in shaping the medical strategy for our organization. As a Clinical Studies Director, you will be responsible for leading the development and execution of medical affairs strategies for our priority programs. This includes developing...

About hVIVOhVIVO is a pioneering company in the field of human-based clinical trial platforms, accelerating drug and vaccine development in respiratory and infectious diseases. Our platform leverages human disease models in flu, RSV, HRV, and respiratory indications, capturing disease in motion and illuminating the entire disease life cycle from healthy to...

About hVIVOhVIVO is a pioneering company in the field of human-based clinical trial platforms, accelerating drug and vaccine development in respiratory and infectious diseases. Our platform leverages human disease models in flu, RSV, HRV, and respiratory indications, capturing disease in motion and illuminating the entire disease life cycle from healthy to...

Job DescriptionJob Title: Senior Medical Writer - Clinical ResearchJob Summary:We are seeking a highly skilled and experienced Senior Medical Writer to join our team at MAC Clinical Research. As a Senior Medical Writer, you will be responsible for creating high-quality clinical study documents, including protocols, informed consent forms, and clinical study...

Job DescriptionJob Title: Senior Medical Writer - Clinical ResearchJob Summary:We are seeking a highly skilled and experienced Senior Medical Writer to join our team at MAC Clinical Research. As a Senior Medical Writer, you will be responsible for creating high-quality clinical study documents, including protocols, informed consent forms, and clinical study...

About the RoleWe are seeking a highly motivated and organized Clinical Operations Specialist to join our team at GlaxoSmithKline. As a Clinical Operations Specialist, you will play a critical role in the planning, execution, and monitoring of clinical trials.Key ResponsibilitiesAssist in the development and implementation of clinical trial protocols and...

About the RoleWe are seeking a highly motivated and organized Clinical Operations Specialist to join our team at GlaxoSmithKline. As a Clinical Operations Specialist, you will play a critical role in the planning, execution, and monitoring of clinical trials.Key ResponsibilitiesAssist in the development and implementation of clinical trial protocols and...

Position Title: Clinical Trials Manager - BiotechContract Type: 12 month contractLocation: London - 3 days onsite requiredKey Responsibilities:Possess over 5 years of pertinent clinical or related experience within the life sciences sector.Hold a Master's degree (MA / MS) accompanied by a minimum of 3 years of relevant clinical or related...

Job Description**Job Title:** Clinical Studies Manager**Job Summary:** We are seeking a highly skilled Clinical Studies Manager to join our team at Advanced Accelerator Applications (Italy) - S.p.A. The successful candidate will be responsible for leading the development and execution of medical affairs strategies for our renal priority programs.Key...

Job Description**Job Title:** Clinical Studies Manager**Job Summary:** We are seeking a highly skilled Clinical Studies Manager to join our team at Advanced Accelerator Applications (Italy) - S.p.A. The successful candidate will be responsible for leading the development and execution of medical affairs strategies for our renal priority programs.Key...

Job Overview:As a Clinical Project Manager at IQVIA, you will be responsible for leading the operational aspects of clinical trials from study start-up to close-out. You will act as the primary point of contact to manage and coordinate the conduct of clinical trials in accordance with ICH-GCP and other applicable local regulations.Key...

Job Overview:As a Clinical Project Manager at IQVIA, you will be responsible for leading the operational aspects of clinical trials from study start-up to close-out. You will act as the primary point of contact to manage and coordinate the conduct of clinical trials in accordance with ICH-GCP and other applicable local regulations.Key...

About the Role:As a Medical Director at Pharma Search, you will play a crucial role in shaping the future of our client's clinical research endeavors. With a proven track record of success, you will be responsible for ensuring the execution, planning, and management of clinical studies to the highest standards across the region.Key Responsibilities:Develop...