IQVIA Biotech is a unique division specialising in working with smaller biotech and emerging biopharma clients and as such we have a vibrant, fast-paced working environment.
The sector we are in is cutting edge for therapies with un-met medical need.
Clinical Trial Managers at IQVIA Biotech are responsible for the planning, implementation and execution of contracted clinical monitoring activities.
They are functionally responsible for all clinical monitoring team members throughout the duration of each clinical trial.
Responsibilities of this role include :
Working closely with the Project Manager to define programme targets for clinical monitoring staff and ensure work is documented within the contracted project scope.
Development and implementation of Clinical Monitoring Plan.
Responsibility for ensuring the needs of the clinical sites are met by facilitating the monitoring processes
Coordination and oversight of daily operations of the clinical monitoring team.
Management of project milestones and proactively address deficiencies
Management of CRA performance
Requirements
BSc degree or equivalent in Life Sciences / Nursing
Prior experience as trial / study manager or strong background as Lead CRA
Thorough knowledge of clinical research process
Prior experience as Clinical Research Associate
Strong communication skills
Fluency in spoken and written English
Excellent organisation and interpersonal skills
Ability to manage multiple priorities
Understanding of basic data processing functions, including electronic data capture
Ability to work independently, prioritise and work within a matrix team environment
This role is permanent, full time and home based in the UK or EU.
We are particularly interested in candidates with oncology or medical devices experience plus at least one of cardiovascular, neurology, immunology, dermatology or internal medicine.
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