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Senior CRA, Hertfordshire

Working for a US Biotechnology organisation that is about to begin UK operations you will be responsible for the hands-on management and monitoring for a number orphan of disease studies being carried out at multiple sites around the country. Orphan disease experience will be useful but not essential. Candidates will require very strong monitoring experience.

For further details please contact Jim Gleeson at jgleeson@ckclinical.co.uk or on 01438 870027

 

 

Biosample Operations Manager, Hertfordshire

A one year contract with a global pharmaceutical company. You will plan and coordinate all operational activities for the collection from Investigator Sites and delivery to laboratories of clinical trial biological samples. Candidates will need previous experience in a clinical trials role gained within a Pharmaceutical Company, Biotechnology Organisation or Clinical Research Association.

For further details please contact Jim Gleeson at jgleeson@ckclinical.co.uk or on 01438 870027

 

 

Senior Contracts and Proposals Manager, West Sussex

This is a permanent position with a large Clinical Research Organisation. The successful candidate will oversee and manage all contract and proposal activities. Responsibilities will include contract preparation, generating payment schedules, analysing internal budgets and managing junior staff.

For further details please contact Jim Gleeson at jgleeson@ckclinical.co.uk or on 01438 870027

 

 

Clinical Study Manager, Epidemiology, Middlesex

A six month contract (initially) with a blue chip Pharmaceutical Company. You will project manage two large Observational Studies in support of a product soon to come to market. Dependant upon experience the successful candidate may also have involvement with some smaller emerging market studies. Previous experience of epidemiological or observational studies is required.

For further details please contact Jim Gleeson at jgleeson@ckclinical.co.uk or on 01438 870027

 

 

Clinical Research Associate, Midlands, 12 month contract 

This is an excellent opportunity for an experienced Clinical Research Associate to join a large Pharmaceutical Company based in the Midlands. You will be employed under an initial 12 month contract and will be responsible for selection, preparation, initiation, monitoring and closure according to Procedural Documents and ICH-GCP as well as local regulations.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

 

 

Clinical Research Manager II, Uxbridge, 11 month rolling contract 

This is an excellent opportunity for a Clinical Research Manager to join one of the worlds largest Biotechnology Companies. You can be based in either Uxbridge or Cambridge and will be employed under an initial 11 month contract. Your responsibilities will include planning and managing clinical operations for assigned clinical projects, including timelines, budgets, personnel resources, investigational sites, vendors and key project deliverables. You will provide strategic planning expertise, draft the operations components and ensure operational feasibility of clinical development plans and scenarios, including budget and resource estimates.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

 

 

Clinical Project Manager, Bucks, Permanent 

This is an excellent opportunity for an experienced Clinical Project Manager to join a medium sized Pharmaceutical Company based in Buckinghamshire. Your main responsibilities will be to discuss, devise and assess the viability of proposed clinical trials and produce study definition documents/study protocols for approval.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

 

 

Clinical Trial Administrator, Bracknell, 12 month contract

This is an excellent opportunity for a CTA to join a large Pharmaceutical Company based in Bracknell. Employed under an initial 12 month contract, you will be responsible for all aspects of administration in line with department objectives and to provide administration support for a number of Clinical Studies conducted by the UK Operating Unit (OPU) from study development, through conduct to reporting according to Standard Operating Procedures.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

 

 

Clinical Research Nurse, North West, 12 month contract

An opportunity to join one of the world’s largest Pharmaceutical Companies on a new initiative. You will work with identified centres in community pharmacy and primary care practice to drive study compliance. You will perform study visits with patients who have volunteered for the study. The ideal candidate will have proven experience in the area of respiratory disease, with a proven track record of being able to work as a team player.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

 

 

Clinical Quality Auditor, Surrey, Permanent

This is an excellent opportunity to further your career within Clinical Quality Assurance with a leading international Pharmaceutical Company. This is a six month contract position, which will be based at our client’s offices in southern England. This is a global role requiring extensive foreign travel, often for a week or more. You will plan, carry out and report on quality audits both internally and of studies contracted to third party suppliers. The successful candidate will also work closely with international regulatory authorities both to stay abreast of developments in their requirements and to facilitate their inspection processes.

For further details please contact Jim Gleeson at jgleeson@ckclinical.co.uk or on 01438 870027

 

 

Senior Associate – Study Management, Uxbridge or Cambridge, 11 month rolling contract

A global Biotechnology Company requires a Senior Associate of Clinical Operations to be based in either their Cambridge or Uxbridge offices. You will be responsible for monitoring of study deliverables and performing protocol related site management activities, participating in study planning and set-up activities including vendor management, project management and coordination of study and implementation plans, contributing to the preparation and/or review of clinical protocols, amendments, consent forms, study guides, monitoring plans, CRFs and subject information sheets, identifying clinical trial investigators and providing clinical site/CRA support by answering protocol-specific questions.

For further details please contact Susan Murray at smurray@ckclinical.co.uk or on 01438 870011

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