Company: RBW Consulting
Closing Date: 23 Dec 16
Salary (£): 40,000 - 60,000
This role is a risk based monitoring opportunity only travelling up to 30% to sites, the rest of your monitoring will be remote, homebased. Thsi role is single sponsor, outsourced to a pharmaceutical company!!
We have an exciting opportunity for developing your skills in Clinical Research as a CRA based in the UK, if you are interested in a new challenge then this role will be ideal for you!
The successful candidate will have the opportunity to work across numerous complex trials within a broad spectrum of therapeutic indications, and will receive outstanding continued provision and training to aid you with the best progression within the organisation.
Monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards.
Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
Assist with study protocol design, development and / or review if required
Complete and compile all necessary research, documentation and information to gain appropriate regulatory and ethical committee approval where required
Perform pre-study initiation, interim monitoring and close out visits as required
Carry out drug formulation administration procedures and documentation records
Ensure adequacy of drug shipment and drug accountability
Liaise with the Medical Monitor, Principal Investigator, clinical operations staff and sponsor representatives as required
Organise/attend investigator meetings as required
Provide support to the Project Manager / Country Manager with ad-hoc tasks as required
Ideal Candidate Profile:
Active development in at least two therapeutic areas
Positive working both independently as well as in a team
Some skills within leadership actions
Ability to review protocols, CRFs and other Project- related data collection tools
Capability to develop and maintain BMS and other related tracking systems
Good communication skills to discuss, present results in meetings to senior members or trial statisticians
This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be. Please contact Sayful Islam on +44 (O)1293 584 300 or email a CV to sayful.islam@rbwconsulting .com.
Keywords: Clinical Research Associate Senior CRA project manager contract clinical trials CRA II clinical research clinical cra, scra, cpm, clinical, clinical research, clinical research associate, pharmaceuticals, biotech, cro, pharma, senior clinical research associate. UK, United Kingdom, England, Scotland, Wales, Northern Ireland
Southdown House, 130a Western Road, Brighton BN1 2LA
|Tel:||01293 584 300|
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