Clinical Support Associate
- Experience Level
- Entry level
Full Time or Part Time (4 days/week) considered.
Location is at the side of the motorway at junction 4 of the M3. Frimley Business Park
The office is moving to White City in West London in November 2019 and the role is 100% office based in both Camberley (now) and in London after the move.
Reporting to the Clinical Support Manager you will be based in a fast paced and dynamic clinical operations group in the UK. The UK affiliate operations group (TMO) is associated with the set up and management of multi therapeutic area clinical trials accross the UK and Ireland (Phase I to IV) including Oncology.
This position would suit a graduate or a junior clinical operations associate/administrator. It is ideal for the first step into commercial operations and there is a real opportunity for career development within the model.
Supports Clinical Project Teams to ensure good quality output for in-house clinical functions within UK Operations
Works closely with In-House Set Up Team and Project Manages to improve rapid study start up and reduce study start up timelines
Proactively assists Project Managers in running of clinical studies and supports field based CRA teams to max-imise study performance
Has a good knowledge of ethics / R&D processes to ensure owned studies are on track
Key, pivitol member of the clinical team to ensure support and communication between project teams
Central point of contact for study related issues across medical and other departments within UK Operations
Ensures all Safety Information for specified trials are distributed to investigational sites according to SOPs and NIPs and prevailing law
Peforms site visits when requested to assist with monitoring activities in the field, unblinded monitoring and drug accountability to improve productivity within the department
Is responsible for ensuring that Investigator payments are made on time and are accurately processed and has an excelllent knowledge of finance systems.
Ensures all trial documentation is created, distributed, maintained and tracked, using electronic storage facili-ties (e.g. CREDI) where necessary, in accordance with SOPs, NIPs and WPs in order to ensure smooth and timely running of trials
Life Science Degree or equivalent.
Desired experience within the Pharmaceutical Industry / CRO enviroment with a good knowledge of Clinical Research processes including ICH GCP
Excellent communication skills and an ability to multi task
PC Literate - Intermediate Word, Excel, Powerpoint, Lotus Notes
key words, clinical trials, graduate, science graduate, clinical support, CTA, clinical trials administrator, study management, administration, clinical research,
Please call Marc Joseph on 01753 216664 for further discussion OR send your CV and application to firstname.lastname@example.org
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