job details for:
Pharmaceutical – Senior Clinical Research Associate (SCRA) Jobs - Manchester

Pharmaceutical – Senior Clinical Research Associate (SCRA) Jobs - Manchester (Job Ref: WR/JOBS/22974-9368)

Job Description :

Flame Pharma Pharmaceutical – Senior Clinical Research Associate Job - Manchester:

Job Summary

We require an experienced Clinical Research Associate (CRA) to work for a world leading, pioneering biopharmaceutical organisation.  Based in Manchester, at the heart of a thriving centre for pharmaceutical research, our client has a drug development portfolio that have reached phase II and phase III of clinical development, as well as a rich pipeline at all stages of pre-clinical R&D.  As a result of expansion, we are recruiting a Senior Clinical Research Associate.

Job Title

Clinical Project Manager

Background

Due to expansion of their drug development portfolio, the Senior CRA will manage a programme of clinical trials, and related activities, to support the research, development and registration of company products.

The Senior CRA will manage a selection of clinical research trials as allocated by the Clinical Project Manager and ensure that Clinical Trial related activities are carried out in accordance with the appropriate Good Clinical Practice (GCP) guidelines and any other relevant guidelines and legislation.

Key Responsibilities:

• Co-ordination of the setting up, running and reporting of Clinical Trials from inception to reporting and / or publication of results
• Assessment and selection of external clinical trial sites
• Production or co-ordination of the production of Clinical Trial Plans, protocols, CRFs and all other trial related paperwork, ensuring where appropriate internal and external approvals are obtained prior to trial commencement
• Management and co-ordination of all required processes during the live phase of a clinical trial
• Monitor clinical trial centres and associated institutions and areas; where appropriate co-monitor with and / or oversee monitoring by CRO staff
• Ensuring that trial non-conformities are identified are dealt with appropriately, both internally and externally
• Write or coordinate the writing of clinical trial reports
• Train or assist in the training of contracted and site staff in ICH / GCP guidelines, and trial or Company related processes and procedures
• Ensure up to date systems (SOPs) are in place to comply with GCP and regulatory guidelines and legislation. Continually monitor the SOP system to both ensure maintained compliance and improve department effectiveness

Experience and Qualifications

• This is a role for an experienced clinical research professional; proven extensive experience in clinical research is likely to be required to effectively carry out this role
• Previous experience as a CRA is essential

Benefits

With this position comes an attractive benefits package that you associate with a world leader, plus a very attractive salary.

Keywords:

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

The position will be based in Manchester.

For further information about this role, please contact Flame Pharma.