An excellent opportunity for experienced Clinical Research Associate to work as a CRA II or Senior CRA with one of the Top 5 CRO. Our Client serves some of the best-known Pharmaceutical companies in the world and work on the most advanced Projects in Drug Development.
We are looking for CRAs with a minimum of 12 months of independent monitoring experience. Should have essentially worked on Phase II, III and Late Phases.
Key responsibilities:

Undertake monitoring (Phase II, III and Late Phase) of Study sites in accordance with current ICH/GCP guidelines, local regulatory requirements and SOPs.
Liaise with the study sites from study start-up to study close-out whilst maintaining relationships with investigators, co-coordinators and the internal project team.
You will also be involved in tracking the Regulatory Authority submissions, Reviewing reports, Site Status, Creating CRF and overlook clinical study Data Processing.


Essential Skills:
• Working experience in the Therapeutic area of Oncology, Cardiovascular, CNS
• Advanced knowledge of GCP/ICH and applicable regulatory guidelines
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
• Effective time management skills and ability to manage competing priorities

Qualification Required:
• Bachelor's degree in a health care or other scientific discipline.

Our client is offering World-Class opportunities for Career Growth and a competitive salary package including fantastic benefits. All these roles can be field-based or office based to suit your requirements

To apply for this position please send us an updated copy of your CV at xxxxxxx.xxxxx@xxxxxxxxx.xxx or call me at 0115 935 2201 for a confidential discussion on this role.

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