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Job Details

Site Manager

Company: Docs Global (Continental Europe)
Location: West Coast,Belgium
Reference: Ref AS-025112
Closing Date: 20 May 18
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

A great opportunity to work in a leading International Pharmaceutical Company as CRA.


Roles & Responsibilities of the position

Responsible for the support and management of study sites for Phase II- IV clinical studies according to SOP’s, GCP regulations and protocol requirements. Identify, evaluate and recommend potential study sites for participation based on feasibility Perform pre-trial assessment visits and coordinate site initiation visits Assures that site personnel complete and document protocol-specific training Conducts on-going study visits and perform Monitoring visits on a routine basis Performs source documentation as required by SOP to ensure protocol/patient compliance Reports any site issues to Clinical Team Ensures that Trial Centre File (TCF) is current up to date Performs drug accountability and any re-labelling that may be required Responds to site questions and escalates as necessary for resolution Attends investigator meetings Participate in QA or FDA audits when necessary

Job Requirements

Education: BSN/BS/MS or BA required Experience: a minimum of two years Clinical Research experience Knowledge of Microsoft Office applications especially Excel English: Fluent spoken & written Fluent n French is a plus Good interpersonal skills demonstrated as proactive, enthusiastic, and independent thinker Ability to collaborate and build strong relationships with all functions involved in the trial Works and meets deadlines with some supervision

Remuneration & other details

We offer a permanent contract, full time and home based role. To apply please send your CV to

Apply for this job: Site Manager

Contact Information:

Address:  Head Office
2 Globeside, Globeside Business Park
Website:  Visit Our Web Site

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