Clinical Trial Associate Team Lead
2 days ago
As a Clinical Trial Associate (CTA) Team Lead, you will be responsible for leading and managing a team of CTAs globally, providing mentorship and guidance to ensure the team's support of clinical study teams. Your strong stakeholder management skills and experience in team leading will be crucial in this role.
You will work closely with Clinical Development teams, Strategic Partner Clinical Research Organizations, and other key stakeholders to ensure the successful delivery of clinical trials alongside the optimization of CTA processes and TMF health.
Key Responsibilities:
- Lead, shape, and develop a team of Clinical Trial Associates globally (both employees and contractors)
- Provide mentorship, guidance, and support to all CTAs
- Ensure internal processes are fit for purpose to support the CTA group and reshape where needed
- Partner with internal and external stakeholders to ensure improvement in collaboration with our CROs, driving responsibilities and accountabilities
- Find efficiencies between UCB systems and Partner systems (e.g., CTMS, Source Quality, SharePoint, MS Teams)
- Support the implementation of new technologies/systems in clinical trials
We are looking for candidates with a Bachelor's Degree and strong knowledge and understanding of the Clinical Development process. In-depth knowledge of TMF systems and processes is also essential. Experience in Project Management techniques and tools is highly desirable.
-
Clinical Trial Associate Team Lead
1 week ago
Slough, Slough, United Kingdom UCB Full timeJob DescriptionWe are seeking a seasoned Clinical Trial Associate (CTA) Team Lead to join our Global Clinical Science and Operations team, based in Brussels, Belgium. As a subject matter expert on TMF systems and processes, you will lead and manage a team of CTAs globally, providing mentorship and guidance to ensure the team's support of clinical study...
-
Clinical Trials Manager
2 weeks ago
Slough, Slough, United Kingdom UCB Full timeAbout the RoleWe are seeking a highly experienced Clinical Trials Manager to lead our Global Clinical Science and Operations team in Brussels, Belgium. As a subject matter expert on TMF, you will be responsible for managing a team of Clinical Trial Associates globally, providing mentorship and guidance to ensure the team's support of clinical study teams.The...
-
Global Trial Operations Director
2 weeks ago
Slough, Slough, United Kingdom UCB Full timeAbout the TeamWe are a dynamic team of professionals working together to deliver clinical trials that make a difference in people's lives. As a Global Trial Operations Director, you will be responsible for leading and managing a team of Clinical Trial Associates globally, providing mentorship and guidance to ensure the team's support of clinical study...
-
Slough, Slough, United Kingdom UCB Full timeJob TitleClinical Trial Associate Team Lead - Neurology ExpertAbout UsUCB is a global biopharmaceutical company focused on neurology and immunology. We have a diverse range of products and services that aim to improve the lives of people affected by serious diseases.Job ResponsibilitiesThe successful candidate will be responsible for leading a team of...
-
Clinical Trials Coordinator
5 days ago
Slough, Slough, United Kingdom Verbatim Pharma Full timeJob Overview:We are seeking a highly skilled Clinical Trials Coordinator to join our team at Verbatim Pharma. As a key member of our operations department, you will be responsible for managing real-world data projects and working closely with clients and internal stakeholders.About the Role:This is an exciting opportunity to work with clients and internal...
-
EU Licencing Team Lead
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeJob Overview:Blackfield Associates is an international pharmaceutical innovation company seeking a skilled Senior Manager Regulatory Affairs to join their EU licencing team in Slough. As a member of the team, you will play a critical role in developing and implementing regulatory strategies to bring innovative medicinal products to market. Key...
-
Slough, Slough, United Kingdom UCB Full timeAbout the OpportunityUCB is a global biopharmaceutical company, focusing on neurology and immunology. We have around 8,500 people in all four corners of the globe, inspired by patients and driven by science.In this role as a Clinical Trial Associate (CTA) Team Lead, you will have the opportunity to lead a team of CTAs globally and contribute to the...
-
Global Regulatory Submission Lead
2 weeks ago
Slough, Slough, United Kingdom ClinChoice Full timeAbout the Role:ClinChoice is looking for a skilled Global Regulatory Submission Lead to oversee the development and implementation of regulatory strategies for EU clinical trials. This role involves leading regulatory activities, developing regulatory strategies, and managing interactions with regulatory authorities.Key Responsibilities:– Develop and...
-
Senior Regulatory Affairs Lead
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeCompany OverviewThe international pharmaceutical innovation company Blackfield Associates is seeking a highly skilled Senior Regulatory Affairs professional to join their EU licensing team based in Slough. Job DescriptionThis permanent position involves developing and leading regulatory strategies for innovative medicinal products throughout the development,...
-
Regulatory Affairs Lead Position
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeJob OpportunityWe are seeking an experienced Regulatory Affairs Lead to join our team at Blackfield Associates. As a Senior Regulatory Affairs Manager, you will play a key role in driving our EU licensing efforts and shaping regulatory strategies.About the JobYou will be responsible for leading the development and implementation of regulatory strategies...
-
Clinical Data Analyst Lead
2 weeks ago
Slough, Slough, United Kingdom Verbatim Pharma Full timeAbout the Role:We offer a competitive salary of £65,000 - £85,000 per annum, depending on experience, for this Data Manager position. If you have previous experience working as a data manager with Clinical trial / Real World Data experience, strong proficiency with EDC platforms for clinical data collection, and a deep understanding of data management...
-
Lead Regulatory Specialist
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeSenior Regulatory Affairs PositionWe are seeking a highly skilled Senior Regulatory Affairs professional to join our EU Licensing team at Blackfield Associates, a renowned international pharmaceutical innovation company.Job Overview:Lead regulatory affairs functions across product development, approval, and lifecycle management.Build and maintain strong...
-
EU Medicinal Product Manager
5 days ago
Slough, Slough, United Kingdom Blackfield Associates Full timeAbout the Opportunity:Our client, Blackfield Associates, is seeking a highly skilled Senior Regulatory Affairs Manager to join their EU licensing team.The successful candidate will be responsible for developing and implementing regulatory strategies for medicinal products across the EU. This includes supporting Clinical Trial Applications, registering new...
-
Clinical Injury Solicitor
3 weeks ago
Slough, Slough, United Kingdom William James Recruitment Full timeExceptional Opportunity for Clinical Negligence SolicitorsWe are seeking an experienced Clinical Negligence Solicitor to join our team in Slough. As a specialist in Clinical Negligence, you will handle high-quality cases from inception through to trial/settlement.The ideal candidate will have a strong legal background, excellent organisational skills, and a...
-
Clinical Negligence Specialist
2 weeks ago
Slough, Slough, United Kingdom William James Recruitment Full timeJob OverviewWe are seeking an experienced Clinical Negligence Solicitor to join our team in Slough, with a salary of up to £60,000.The RoleThis is an exceptional opportunity for a dedicated professional to handle high-quality clinical negligence cases from inception through to trial/settlement.The ideal candidate will have experience in clinical negligence...
-
Regulatory Affairs Director
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full time**Job Title:** Senior Manager Regulatory Affairs We are seeking a highly experienced Senior Manager Regulatory Affairs to join our EU licencing team at Blackfield Associates. This is a permanent position with hybrid working from Slough, where you will be required to attend the office on a weekly basis. About the Role:The successful candidate will develop...
-
Regulatory Affairs Director
3 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeSenior Regulatory Affairs ManagerWe are seeking an experienced Senior Regulatory Affairs Manager to join our EU Licensing team at Blackfield Associates, a leading international pharmaceutical innovation company.About the Role:Develop and lead regulatory strategies throughout product development, approval, and lifecycle management.Serve as the primary point...
-
Regulatory Affairs Strategy Leader
3 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeCompany OverviewBlackfield Associates is a leading international pharmaceutical innovation company with a presence in the EU. We are seeking an experienced Senior Regulatory Affairs Manager to join our EU licensing team.About the RoleWe offer a competitive salary of £80,000 - £110,000 per annum, depending on experience, and a comprehensive benefits...
-
Clinical Negligence Specialist
2 weeks ago
Slough, Slough, United Kingdom William James Recruitment Full timeAbout the RoleClinical Negligence Solicitor - Slough – Estimated Salary: £60,000 per annumWe are seeking an exceptional Clinical Negligence Solicitor to handle high-quality cases from inception through to trial/settlement.The ideal candidate will bring experience in Clinical Negligence claims, with a proven ability to investigate and litigate multi-track...
-
EU Regulatory Affairs Director
2 weeks ago
Slough, Slough, United Kingdom Blackfield Associates Full timeRole SummaryWe are seeking a highly experienced EU Regulatory Affairs Director to join our team at Blackfield Associates. As a Senior Regulatory Affairs Manager, you will lead our EU licensing efforts and drive regulatory strategies.About the RoleYou will be responsible for developing and implementing regulatory strategies during product development,...