CTA/Clinical Trials Administrator

Recruiter
Chiltern
Location
Berkshire
Posted
19 Jan 2018
Closes
18 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Job Summary: This is 100% office based in Bracknell. Requirements: We are looking for an experienced/career CTA. This is NOT a junior/trainee role. We MAY consider someone 4 days/week if you hit the mark. You would be employed on a permanent basis by Chiltern on PAYE and seconded to the pharma company on a rolling 12 monthly contract. Benefits include :- 25 days leave Pension Life Insurance Contributions towards health/dental/optical costs Gym subscription contribution Flexi time – core hours are 10 till 3 One day a month the department goes out to do community/charity work – group bonding etc. Lots of team building days/activities Personable/friendly team – large open plan office Very high/strong contract culture and virtually no difference for perm staff versus contractors in the way they are treated/rights etc. They have free car parking on site. Restaurant/coffee shop access Someone who wants to stay long term/career CTA would be ideal DUTIES:- To 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 UK Operating \Unit (OPU) from study development, through conduct to reporting according to Standard Operating Procedures and ICH-GCP. Act as a focal point for a therapy group and coordinate group activities by (for example): - diary management - handling and resolving internal and external queries Provide administrative support to a therapy group, to include: - initiating, typing and editing of correspondence - assisting with the production and writing of Clinical Trial reports - compiling presentations Co-ordinate and dispatch essential trial documents Create and update appropriate tracking systems CTMS: - complete trial site details for investigators and ethics committees for designated therapy group - provide reports to Clinical Monitor as appropriate to ensure awareness of milestones Ensure all essential supplies and documents required for the smooth running of a study are available and in place Liaise with other CTAs to ensure adequate local cover/support is available when required Ensure SAEs are handled as a priority and in accordance with Company Policy Ensure appropriate archiving of documentation PLEASE APPLY BY SENDING YOUR UPDATED CV IN THE FIRST INSTANCE to marc.joseph@chiltern.com OR via the link on pharmiweb. Alternatively please feel free to give Marc a call on 01753 216664 to discuss the role further. key words CTA, clinical trials administration, in house CRA, documentation, clinical trial administrator

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