Clinical Study Associate Manager
2 days ago
Are you a detail-oriented and organized individual looking for a challenging role in clinical research? We are seeking a Clinical Study Associate Manager to join our team at Medpace. In this role, you will be responsible for managing multiple clinical studies from initiation to closeout.
Responsibilities:- Oversee site initiation, monitoring, and closeout activities to ensure compliance with study protocols;
- Collaborate with cross-functional teams, including clinical operations, data management, and statistical analysis;
- Develop and maintain effective relationships with sites, vendors, and internal stakeholders;
- Identify and mitigate risks associated with clinical trials;
Requirements:
- Masters degree in a health or life science related field preferred;
- Minimum of 2 years experience in clinical research management;
- Strong analytical and problem-solving skills;
- Valid driver's license required;
Salary Range: $80,000 - $110,000 per year
Benefits:
- Competitive compensation package;
- Flexible work environment;
- Structured career paths with opportunities for growth;
About Medpace:
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
-
Global Study Associate
4 days ago
London, Greater London, United Kingdom Medpace Full timeAbout the PositionWe are looking for a Global Study Associate to join our Clinical Trial Management team at Medpace. As a Global Study Associate, you will play a key role in ensuring the timely delivery of recurrent tasks and maintaining accurate records within the clinical trial management system.The ideal candidate will have a strong understanding of...
-
Associate Clinical Study Manager
4 days ago
London, Greater London, United Kingdom ""Veristat, Inc. Full timeJob Summary:As an Associate Clinical Study Manager at Veristat, Inc., you will have the opportunity to work on complex projects and develop your skills in statistical programming.We are looking for a skilled professional with a Master's degree in technology, statistics, pharmaceutics or a related field, and 5 years of SAS programming experience.About the...
-
Clinical Study Manager Senior
4 days ago
London, Greater London, United Kingdom BIOMARIN Full timeBioMarin Job Opportunity: We are seeking an experienced Associate Clinical Study Manager to join our team at BioMarin. The ideal candidate will have a strong background in clinical research and a passion for driving innovative medical solutions.About the Role:This is an exciting opportunity for a highly motivated individual to take on a leadership role...
-
Clinical Research Associate
2 days ago
London, Greater London, United Kingdom IQVIA Full timeIQVIA UK is seeking experienced professionals to strengthen our client-facing service team as a Clinical Research Associate. This role will involve performing site monitoring visits, managing study progress, and collaborating with the study team.ResponsibilitiesWe are looking for candidates who have experience in independent on-site monitoring in the UK,...
-
Senior Clinical Study Manager
1 month ago
London, Greater London, United Kingdom BIOMARIN Full timeJob SummaryWe are seeking a highly skilled Senior Clinical Study Manager to join our team at BioMarin. This role will be responsible for leading clinical programs across various phases, from proof-of-concept to Phase 3 and BLA/NDA/MAA filing.About UsBioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic...
-
Clinical Science Associate Manager
4 weeks ago
London, Greater London, United Kingdom BioMarin Pharmaceutical Inc. Full timeBioMarin Pharmaceutical Inc. is a leading biotechnology company that applies its scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines.We are seeking an experienced Associate Medical Director, Clinical Science to join our team in San Rafael, CA. The ideal candidate will have 2 or more years of...
-
Clinical Study Specialist
2 weeks ago
Uxbridge, London , Uxbridge, London, London, United Kingdom Regeneron Full timeThe Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution of one or more studies across a program. The CSS receives assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will support...
-
Global Study Associate
4 days ago
London, Greater London, United Kingdom Medpace Full timeJob DescriptionWe are seeking a Global Study Associate to join our team in London. The successful candidate will be responsible for supporting the management of clinical trials, ensuring timely delivery and high accuracy.Key ResponsibilitiesCommunicate and collaborate with global study teamsCompile and maintain project-specific status reportsProvide...
-
Clinical Studies Manager
3 weeks ago
London, Greater London, United Kingdom University College London Hospitals Full timeJob DescriptionWe are seeking an experienced Clinical Studies Manager to join our team at University College London Hospitals (UCLH). The successful candidate will have a strong background in clinical trials and will be responsible for the coordination and management of a portfolio of studies.Key responsibilities will include:Education of patients and...
-
Study Management Specialist
4 days ago
London, Greater London, United Kingdom Medpace Full timeAre you passionate about applying your academic expertise in clinical project administration and management? Medpace is recruiting an Associate Clinical Trial Manager to join its London-based team, focusing on renal-related projects.Annual Salary Range: $100,000 - $130,000As a key member of the clinical trial management team, you will collaborate with the...
-
Associate Clinical Research Manager
4 days ago
London, Greater London, United Kingdom Medpace Full timeWe are seeking an experienced Associate Clinical Research Manager to join our team at Medpace, offering a highly competitive salary package of $85,000 - $120,000 per year.In this role, you will work closely with project coordinators and clinical trial managers to ensure seamless execution of clinical trials.Your key responsibilities will...
-
Clinical Research Associate
4 days ago
London, Greater London, United Kingdom The Institute Of Cancer Research Full time**Job Title:** Clinical Research Associate**Location:** SuttonWe are seeking a highly motivated and organized Clinical Research Associate to join our dynamic clinical trials unit. As a Clinical Research Associate, you will be responsible for providing administrative support to the Clinical Trials' Team and supporting the team in the processes of data...
-
Clinical Trials Physician
2 days ago
London, Greater London, United Kingdom Medpace Full timeClinical Trials Medical Director OpportunityWe are seeking an experienced Oncologist to fill the role of Medical Director at Medpace. As a Medical Director, you will provide medical leadership and expertise to clinical trials, working closely with cross-functional teams to ensure successful project outcomes.The ideal candidate will have a strong background...
-
Clinical Research Associate Specialist
4 weeks ago
London, Greater London, United Kingdom Meet Full timeJob OverviewMeet your next career challenge as a Freelance Clinical Research Associate (CRA) in our dynamic team. With extensive experience in oncology clinical trials, you will be responsible for monitoring and managing clinical trial sites to ensure compliance with protocols, regulatory guidelines, and study timelines.This role requires strong project...
-
Clinical Research Associate
4 weeks ago
London, Greater London, United Kingdom Novotech Full timeJob OverviewWe are seeking a highly skilled and experienced Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for managing clinical trials from initiation to close-out.About the RoleAs a Clinical Research Associate, you will be expected to actively participate in and manage the recruitment of potential...
-
Global Study Associate
4 days ago
London, Greater London, United Kingdom Medpace Full timeClinical Research Professional WantedWe are a full-service contract research organization (CRO) that provides clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through our scientific and disciplined approach.We are...
-
Clinical Study Delivery Lead
4 weeks ago
London, Greater London, United Kingdom GSK Full timeJob Description:We are seeking an experienced Clinical Study Delivery Lead to join our team at GSK. As a key member of our Global Clinical Delivery (GCD) team, you will be responsible for planning and leading the delivery of oncology studies to time, quality, budget, company standards, and scientific requirements.The ideal candidate will have extensive...
-
Associate Clinical Trials Management Lead
4 weeks ago
London, Greater London, United Kingdom Medpace, Inc. Full timeWe are seeking an experienced Associate Clinical Trials Management Lead to join our UK, London Clinical Trial Management team. In this role, you will lead the management of clinical trials, providing strategic guidance and direction to the team.The ideal candidate will have a PhD in Life Sciences, extensive experience within the CRO or pharmaceutical...
-
Clinical Study Risk Manager
4 weeks ago
London, Greater London, United Kingdom Lifelancer Full timeJob Description:This position is a key role within our clinical study management process, requiring strong technical and clinical trial expertise to ensure quality oversight of sites, countries, and studies.We are seeking a highly skilled Clinical Study Risk Manager to join our team in the biotech industry. As a RBSM Central Risk, you will contribute to the...
-
Associate Director
2 weeks ago
London, Greater London, United Kingdom Novartis Farmacéutica Full timeAbout the RoleThe Associate Director will be responsible for managing vendor relationships, ensuring quality and service level standards are met, and driving a frontloaded and timely study-start-up process. This is a hybrid office/home based position with 12 days per month to be performed from the White City office.Responsibilities:Close interaction and...