|Salary:||£43,000 to £56,000 per annum|
|Placed On:||13th January 2022|
|Closes:||6th February 2022|
Salary: Starting salary c£43,000.
Salary range £43,000 to £56,000 per annum. Appointments are normally made at the starting salary, however previous experience will be taken into consideration. Future progression is based on annual performance review.
Duration of Contract: Fixed Term for 24 months
Hours per week: 35 (Full Time), flexible working options may be considered.
Summary of Role
The Institute of Cancer Research is looking for an experienced Clinical Trials Programme Manager to join the Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) at its Sutton site in Surrey. ICR-CTSU runs a diverse portfolio of national and international phase III multi-centre randomised controlled trials, and phase II targeted treatment trials, with a special emphasis in breast, urological, lung and head and neck cancer treatments.
The post offers an excellent opportunity for an enthusiastic and well-motivated individual with clinical trial experience to work in a dynamic and supportive academic environment at one of the leading National Cancer Research Institute cancer trials units. The successful candidate will join the ICR-CTSU Management Group and responsibilities will include:
The strategic oversight of a defined programme of research within the ICR-CTSU portfolio;
The development and initiation of new trials;
Providing operational oversight of dedicated trials teams to ensure successful trial delivery.
Applicants should hold a first degree or equivalent level qualification in life science or health related subject and have an in depth understanding of the principles of Good Clinical Practice, Data Protection, Research Governance and the Human Tissue Act. Experience/knowledge of laboratory quality systems and procedures is highly desirable. Excellent interpersonal skills are required, as is the ability to work to high standards across a variety of tasks with constant regard to scientific and regulatory requirements. A proven track record in the planning, coordination and conduct of clinical trials within the NHS or academia, a CRO or a pharmaceutical company is essential
We encourage all applicants to access the job pack attached for more detailed information regarding this role.
Appointment will be on a fixed term contract for 2 years. We currently have a blended approach to home and office working, and flexible working options may be considered.
Informal enquiries can be made by emailing firstname.lastname@example.org.
To apply, please click on the Apply button below and follow the instructions.
When applying please provide a supporting statement detailing why you are applying for this position and detailing your relevant experience; together with your CV including details of your current salary and the names and addresses of two referees.
Type / Role: