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

Clinical Research - Clinical Research Associate (CRA) Jobs - Europe (Job Ref: WR/JOBS/20812-7907)

Job Ref : WR/JOBS/20812-7907
Discipline : Clinical Research/Clinical Research Associates
Contract : Permanent
Salary : £30,000 p.a. €30,000

Vacancy Location : International View Map

Job Description :

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

Job Summary

Flame Pharma have an excellent opportunity for an experienced CRA to join a world leader and become a valuable part of their successful team. Flame Pharma are recruiting on a European scale for Clinical Research Associates (CRA) to work for our client, one of world’s leading Clinical Research Organisations. As an experienced clinical research associate, you will have previous experience within clinical research, and have had responsibility for identification, selection, initiation and close-out of appropriate investigational sites for clinical research studies.

If you are a clinical research associate looking to progress to senior clinical research associate or lead clinical research associate, and even progression onto clinical project manager, then this opportunity is for you.

Job Title

Clinical Research Associate

Background

Our Client have an excellent and exciting yet challenging positions for a Clinical Research Associate to join their team in Europe. The clinical research associate will have responsibility for identification, selection, initiation and close-out of appropriate investigational sites for clinical research studies.

Key Responsibilities

Assist the Clinical Project Manager and Senior Clinical Research Associate with the day-to-day running of international clinical research studies.
Perform Selection, Initiation, Monitoring and Closure Visits at Investigator Sites according to project schedule. Adhere to project guidelines for monitoring requirements.
Facilitate the Import, Delivery and Return of Clinical Trial Medication and other Clinical Trial Materials to Investigator Sites. Monitor the storage and usage of Clinical Trial Materials by Investigator Sites.
Maintain regular and effective verbal and written communication with clinical project management team members and, where appropriate, the Sponsor.
Develop a comprehensive knowledge of the clinical study protocol and other relevant documentation.
Obtain key GCP documents prior to Site Initiation for appropriate filing and distribution.
Maintain updated clinical study Site and In-house files for the duration of the clinical study.
Maintain regular contact with Investigator & Site staff by means of letters, emails and weekly telephone calls. Provide site with necessary study updates and documents. Monitor site adherence to the protocol and regulatory procedures, and provide ongoing site support and training for study procedures.
Develop and maintain a working knowledge of current SOPs and ICH-GCP & FDA requirements.
Attend training courses and seminars as designated by senior clinical management.

Experience and Qualifications

University degree in a scientific discipline (or equivalent)
Working knowledge of ICH GCP and clinical trial methodology
Previous Clinical Research Associate experience within clinical research or Pharmaceutical sectors
Computer literate
Good interpersonal and organisational skills

Benefits

With this position comes an attractive benefits package that you associate with a world leader, including pension, healthcare, plus a salary of €30,000.

Key Words

Clinical Research Associate, CRA, Clinical Project Management, Senior Manager, Clinical Research, Clinical Trials, Medical, Clinical, CRO, Study Management, Clinical Management, Pharmaceutical, Career, Research