Company: SEC Recruitment
Closing Date: 31 Oct 16
Salary (£): Negotiable
Prestigious global client is actively seeking for freelance CRAs for an initially 3 months contract due to be extended.The position is office based and full time.Your major responsibilities will include: ?Obtain and maintain essential documentation in compliance with ICH-GCP. ?Actively participate in Local Study Team meetings. ?Contribute to the selection of potential investigators. ?Train, support and advise Investigators and site staff in study related matters. ...
Prestigious global client is actively seeking for freelance CRAs for an initially 3 months contract due to be extended.
The position is office based and full time.
Your major responsibilities will include:
?Obtain and maintain essential documentation in compliance with ICH-GCP.
?Actively participate in Local Study Team meetings.
?Contribute to the selection of potential investigators.
?Train, support and advise Investigators and site staff in study related matters.
?Contribute to national Investigators meetings.
?Initiate, monitor and close study
?Drive performance at the sites.
?Proactively identify study-related issues, solutions and escalates as appropriate.
?Update IMPACT and other systems with data from centres as per required timelines.
?Manage study supplies (ISF, CRF, etc), drug supplies and drug accountability at study sites.
?Perform source data verification according to SDV plan.
?Ensure data query resolution by the site.
?Ensure accurate and timely reporting of Serious Adverse Events by the site.
?Prepare for activities associated with audits and regulatory inspections in liaison
?Provide monitoring visit reports
Minimum Requirements and Preferred Background
?Minimum University degree and / or equivalent, preferred in biological science or healthcare-related field.
?Fluent knowledge of spoken and written English.
?Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP.
?Good knowledge of relevant local regulations.
?Basic understanding of the drug development process.
?Ability to travel nationally as required.
If you would like to discuss this position further, please contact Agnes: 07912097877 or email: email@example.com.
Key Words: CRA, CRA II, Senior CRA, Lead CRA, Clinical Research, Clinical Operations, Clinical Research Associate, Clinical Research Associate II, Senior Clinical Research Associate, Freelance, Contract, Interim, Phase II, Phase III, Temporary, Contract CRA, UK, Midlands, England, Pharma, Pharmaceutical, Sponsor
SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business.
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