Senior Clinical Study Manager
3 weeks ago
Senior Clinical Study Manager
Permanent Position
Remote (will involve UK and international travel)
Salary up to £80,000 + bonus + competitive benefits
Are you an experienced study manager within clinical research?
Are you looking for a senior, rewarding role within clinical study management in the pharmaceutical industry?
My client are a leader in delivering high quality, processed biological materials across the UK and globe, with a large portfolio of therapeutics at market and in development. Due to continued growth, they are looking to bring onboard a Senior Clinical Study Manager who will take ownership of studies across the business, including a large upcoming international trial.
The Senior Clinical Study Manager will manage the delivery of clinical studies, from study set up through to final report review and submission, interacting with key stakeholders internally and at partner Clinical Research Organisations (CRO’s).
Due to the nature of the role and global presence of the organisation, there will be a requirement for travel within the UK and internationally (Europe and US).
Key responsibilities of the Senior Clinical Study Manager include:
- Oversee and ensure the delivery of phase I to IV clinical trials from set up, through to recruitment, study initiation, close-out and final report submission.
- Ensure successful relationships with external stakeholders and partners are maintained, including Clinical Research Organisations (CRO’s), vendors and at study sites.
- Monitor study timelines, ensuring key milestones are achieved as planned, and addressing any potential risks.
- Manage large study budgets, making decisions on expenditure independently.
- Ensure studies are conducted in accordance with applicable regulatory requirements, standard operating procedures (SOP’s), Good Clinical Practice (GCP).
- Conduct external audits and investigations to maintain regulatory compliance, ensuring the resolution and closure of any findings.
- Provide frequent updates on study status, including at project meetings and within the wider clinical research team.
- Contribute to organisational process improvement initiatives.
To be considered as a Senior Clinical Study Manager, you will need the following skills or experience:
- Significant experience within clinical study management within the Pharmaceutical, Bio-Pharmaceutical or Biotechnology industry, working directly within the sponsor organisation.
- Experience handling large clinical budgets (in the millions), able to make independent decisions on expenditure.
- A strong working knowledge of Good Clinical Practice (GCP) and associated regulatory standards.
- Experience working across Phase I to IV trials.
- Able to plan and manage clinical studies, providing regular reports and updates to ensure projects run to time and budget.
- Excellent communication skills and a personable nature, to support relationship building with stakeholders and cross functional teams.
- Strong written skillset in order to prepare technical scientific reports, documents and presentations.
- BSc/MSc/PhD in a scientific subject (Biomedical Science, Biochemistry, Biology, Pharmaceutical Science, Chemistry etc.) or equivalent working experience.
- Comfortable travelling as needed within the UK, Europe and US.
Please apply online or contact Katie-May Kress at CY Partners for more information.
Keywords: Senior Clinical Study Manager, Clinical Study Manager, Clinical Study Lead, Clinical Trials Lead, Study Lead, Study Manager, Clinical Research, Clinical Studies, Clinical Trial, Good Clinical Practice, ICH-GCP, GCP, GxP, Sponsor, Pharmaceutical, Bio-Pharmaceutical, Biotechnology, CRO, Clinical Research Organisation, Remote, UK, US, Europe”
The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.
-
Senior Clinical Study Manager
3 weeks ago
United Kingdom CY Partners Full time €80,000Senior Clinical Study Manager Permanent Position Remote (will involve UK and international travel) Salary up to £80,000 + bonus + competitive benefits Are you an experienced study manager within clinical research? Are you looking for a senior, rewarding role within clinical study management in the pharmaceutical industry? My client are a leader in...
-
Clinical System Analyst
3 weeks ago
United Kingdom Catalyst Clinical Research Full timeAs a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and procedural development, core system functions, systems...
-
Clinical System Analyst
3 weeks ago
United Kingdom Catalyst Clinical Research Full timeAs a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and procedural development, core system functions, systems...
-
Clinical System Analyst
3 weeks ago
United Kingdom Catalyst Clinical Research Full timeAs a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and procedural development, core system functions, systems...
-
Senior Manager, Clinical Trial Management
3 weeks ago
United Kingdom CY Partners Full time €80,000Senior Clinical Study Manager Permanent Position Remote (will involve UK and international travel) Salary up to £80,000 + bonus + competitive benefits Are you an experienced study manager within clinical research? Are you looking for a senior, rewarding role within clinical study management in the pharmaceutical industry? My client are a leader...
-
Senior Clinical Trial Associate- United Kingdom
1 month ago
United Kingdom Catalyst Clinical Research LLC Full timeAs a Senior Clinical Trial Associate you are responsible for providing the administrative support to the clinical development/project teams and maintaining a range of clinical documentation. You will be focused on supporting external client teams as well as our internal Clinical Services team. You will work closely with project teams to ensure that...
-
United Kingdom Catalyst Clinical Research LLC Full timeAs a Clinical Development Systems Analyst you are a key member of the Business Enablement Team. You will act as a Subject Matter Expert (SME)/Super User in the assigned systems utilized for efficient management and oversight of clinical trials. Supporting Catalyst Clinical Systems process and procedural development, core system functions, systems...
-
Study Manager
2 weeks ago
United Kingdom AstraZeneca Full timeTitle - Global Study ManagerLocation - RemoteIR35 Status - InsideDuration - 12 monthsMake a more meaningful impact to patients’ lives around the globe!Here you’ll have the opportunity to make a meaningful difference to patients’ lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines –...
-
Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timeWe are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...
-
Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timeWe are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...
-
Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timeWe are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...
-
Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timeWe are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...
-
Senior SAS Programmer
4 weeks ago
United Kingdom MAC Clinical Research Full timeWe are seeking a Senior Programmer to work across multiple clinical and non-clinical studies; supporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area;...
-
Senior Clinical Research Associate
3 weeks ago
United Kingdom CCS-Global Full timeSenior CRA1, Senior CRA2, or Lead Level CRAMidlands, South West, or North West Regions (Remote/Field-Based)Full-Time / Part time considered. About the OpportunityWe’re exclusively partnered with a respected leader in clinical research full service provision, as they expand their team, we are actively recruiting for Senior CRA1, Senior CRA2, or Lead CRA...
-
Contract Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timesupporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...
-
Contract Senior SAS Programmer
1 month ago
United Kingdom MAC Clinical Research Full timesupporting regulatory submission activities; producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines. Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area; reviewing Statistical Analysis Plans (SAPs), including study specific ISS/ISE and DSMB SAPs and...
-
Senior Clinical Research Associate
6 days ago
United Kingdom CCS-Global Full timeAbout the CompanyWe’re exclusively partnered with a respected leader in clinical research full service provision, as they expand their team, we are actively recruiting a Clinical Research Associate level 2 or Senior CRA to join their team in the United Kingdom. Our Client is known for its dedication to advancing clinical research and delivering positive...
-
Clinical Programmer
2 weeks ago
United Kingdom AL Solutions Full timeAbout the Role:The Clinical Programmer plays a key role in supporting clinical trials by developing and validating clinical data systems. Key duties include programming study databases, extracting data, and ensuring data integrity and regulatory compliance. This position will collaborate with data managers, statisticians, and researchers to support accurate...
-
Clinical Project Manager
2 weeks ago
United Kingdom PNEUMAGEN LIMITED Full timeThis is a temporary role to cover maternity leave absence for one of our existing Clinical Project Managers. The Clinical Project Manager is responsible for managing our Neumifil clinical program as an influential, capable and credible project management professional. Reporting to the CEO, the Clinical Project Manager has accountability for the clinical...
-
Senior Bioanalytical Manager
4 weeks ago
United Kingdom Next Phase Recruitment Full timeWe are seeking a highly experienced Senior Bioanalytical Manager to lead our cutting-edge clinical laboratory, supporting the development of innovative pharmaceutical products. In this role, you will oversee the development, validation, and application of bioanalytical methods for both clinical and preclinical studies, utilizing advanced techniques such as...