Clinical Trial Manager – Uxbridge, UK. CLUSTER LEVEL ROLE! Maidenhead, England
Job description
Are you a local Study Manager who is looking for the next challenge? If so then this may be the role for you….
Due to continued growth we are continuing to expand our CTM team within a client dedicated FSP role. This role requires you to lead and manage trials and teams across a cluster, so you will be working with teams in the UK, ROI, Belgium and The Netherlands. You will be involved in Oncology studies, managing CAR T trials, however our client also develops innovative solutions to Haematology, Immunology and Cardiovascular diseases.
Other Key duties include:
- Writing Protocols and Consent forms
- Organising Kick off meetings
- Training CRA teams
- Organising INV meetings
- Monitoring and tracking start up activities
- Co-ordinating the submission process and ethics approvals
- Supporting monitoring teams – the CRAs will approach the CPL for advice when needed
- Oversee the monitoring activities e.g. review trip reports, check compliance, co-monitoring
- Developing the strategy, tools and training to oversee and assess the performance of CRA’s – trip report review, monitoring tool compliance, AFV
- Identifying risks, follow up on issues, timely response to audit inspection reports
This particular role is a client dedicated one where you will work exclusively on one sponsor’s trials and SOPs; a client that values their staff and puts an emphasis on career development.
Reasons to apply:
- This client’s team is an extremely happy one, with low attrition rates. For example employees who leave on mat leave are desperate to come back, they simply love working here!
- The Uxbridge office is impressive; modern and well equipped with a great canteen & free parking available
- Free shuttle bus to and from Uxbridge station to the client offices
- Free on-site gym
- Work from home 2 days per week
Requirements:
- A minimum of 5 years experience within Clinical Research
- Experience of Clinical Trial design
- The ability to plan, set and manage Clinical Trial budgets.
- Previous CRA experience in the UK is preferable
Other Information: This role is a full time & permanent position to be employed through Labcorp. Candidates will need to be office based in Uxbridge 3 days per week with home working up to 2 days per week. For more information please contact Andy Smith on + 44 (0)7775 848 250 or mail [email protected]
Key words: CTL, Clinical Team Leader, Clinical Research, lead CRA, Uxbridge UK GCP, Oncology, Diabetes, Rare disease, Office Based Pharmaceutical, Clinical Project Leader, Uxbridge, CTL, Clinical Team Leader, Clinical Research, lead CRA, Reading UK GCP, Oncology, Diabetes, Rare disease, Office Based
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
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