job details for:
Clinical Research - Clinical Research Associate Jobs - Europe (Spain)

Clinical Research - Clinical Research Associate Jobs - Europe (Spain) (Job Ref: WR/JOBS/13260-5521)

Job Ref : WR/JOBS/13260-5521
Discipline : Clinical Research/Clinical Research Associates
Contract : Permanent
Salary : £21,000-31,000 p.a. 22500-46000 Euro

Vacancy Location : International View Map

Job Description :

Flame Pharma Clinical Research - Clinical Research Associate Job - Europe (Spain):

Our client is currently recruiting Clinical Research Associates who are looking to progress their career within Clinical Research, to be based in Barcelona, Spain.

Due to expansion, our client is looking to recruit Clinical Research Associates to identify, select, initiate and close-out appropriate investigational sites for clinical research studies, and to monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with Company SOPs, applicable regulations and the principles of Good Clinical Practice.

Key Responsibilities:

Familiarity with COMPANY Consulting Division SOPs and appropriate regulations
Recruitment of investigators
Co-ordinate all the necessary activities required to set up and monitor a study, including the following:

Identify investigators
Help, when requested, in preparation of regulatory submissions
Design patient information sheets and consent forms
Ensure timely submission of protocol/consent documents for ethics/IRB approval
Placement and initiation visits
Conduct regular monitoring visits in accordance with the COMPANY Consulting Division site monitoring SOP / Sponsor site monitoring SOP, as appropriate
Maintain all files and documentation pertaining to studies
Motivate investigators in order to achieve recruitment targets
Complete accurate study status reports
Ensure the correct storage of drugs and the diligent account of all drugs in accordance with SOPs
Keep the project manager informed
Process case record forms to the required quality standards and timelines
Deal with Sponsor generated queries in a timely manner
Ensure the satisfactory close-out of investigator sites
Participate, if requested, in the preparation of and review of study documentation, e.g. draft protocols, draft CRFs, monitoring guidelines and elements of final report
Ensure correct archiving of files on completion of a study
Co-operate with sponsor and/or COMPANY QA personnel in the conduct of QA audits
Maintain patient and sponsor confidentiality

Cost effectiveness
To participate in training new staff as appropriate
Assist with marketing the company if and when appropriate

Key Requirements:

Medical/science background and relevant experience
1-2 years CRA experience
Ability and willingness to travel at least 50% of the time. (International and domestic: fly and drive)
Ability to review and evaluate clinical data
Computer literacy desirable
Fluent in English plus fluent in local language
Current full driving licence essential
Good oral and written communication skills

With this position comes an attractive remuneration package associated with such a well-established organisation.

Salary of Circa EURO 22,500 to 46,000 depending on experience.

The position will be based in Barcelona, Spain.

For more information, please contact Flame Pharma today.