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Job Details

Clinical Research Associate – General Medicine – Global CRO

Company: i-Pharm Consulting
Location: London
Reference: LMCN2511
Closing Date: 09 Dec 16
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

CRA - Clinical Research Associate - General Medicine - Global CRO - Home-based i-Pharm Consulting is seeking a CRA to work on a permanent basis for an award winning CRO. Focusing on General Medicine trials, the chosen candidate will have the opportunity to progress their career within this dynamic organisation, in a supportive environment with industry leading training resources.

Requirements:

CRA – Clinical Research Associate – General Medicine – Global CRO - Home-based

i-Pharm Consulting is seeking a CRA to work on a permanent basis for an award winning CRO. Focusing on General Medicine trials, the chosen candidate will have the opportunity to progress their career within this dynamic organisation, in a supportive environment with industry leading training resources.

Primary Benefits

• Competitive salary package with a generous car allowance.
• Exposure to a wide range of activities – study start-up (feasibility and ethic submission), site initiation, site recruitment, routine monitoring and study close-out.
• Excellent training and support from a growing colleague base in the UK and continental Europe.
• As my client’s operations continue to expand in the UK, career progression opportunities will certainly be possible and, indeed, an expectation from their employees.

In your new role…

• You will act as the primary liaison between the CRO and the clinical sites, ensuring the overall integrity of the study implementation and the study protocol at the clinical sites.
• You will be conducting monitoring on a range of clinical trials, while attending site visits to ensure GCP-ICH and all study compliance protocols are adhered to.
• You will establish a site recruitment plan, attend audits and complete routine departmental administrative tasks.
• You will conduct remote visits, facilities inspections and on-site study training as necessary, as well as providing support to more inexperienced colleagues.
• You will determine and recommend the appropriate follow-up response to deficiencies in documentation, communication and the need for additional training.
• You will monitor patient safety on an on-going basis and evaluate the overall compliance and performance of sites.

Necessary Experience

• At least 18 months’ independent monitoring experience.
• Educated to a degree level (preferably a health science subject).
• Candidates must have the right to work in the UK.

LOCATION:

UK, home-based role

SALARY:

- From £30,000 to £45,000 depending on experience
- Competitive bonus scheme
- Comprehensive benefits package

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.i-pharmconsulting.com

TO APPLY

If you would like to discuss this vacancy further, please call Recruitment Consultant Lauren on +44 (0)20 3189 2295, or email lmccollum@i-pharmconsulting.com. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

KEY WORDS

CRA / Monitoring / Pre-study / Initiation / Close-out / Study Start-up / Ethics / Feasibility / GCP / ICH / Clinical Research Associate / Budget Negotiation / London / Uxbridge / Slough / South East / Berkshire / Slough / Hayes / Windsor / Heathrow / M4 / M25 / Wokingham / High Wycombe / Birmingham / Manchester / Scotland / Wales / Cardiff / Newcastle / Cambridge / Oxford / Leeds / Reading / Southampton / Liverpool / North West / Northern Ireland / Ireland / Bristol / Liverpool / Somerset / Wiltshire / Kent / Essex / Sussex / Surrey / Camberley / Crawley / Edinburgh / CRA I / CRA II / CRA III / SCRA / Home-based / Contract Negotiation / Site Identification / Science / Pharma / Pharmaceutical / Permanent / SOP / Clinical / Clinical Research Associate I / Clinical Research Associate II / Clinical Research Associate III / On-site / Remote Visits / Study Implementation / Protocol / Site Regulatory Package / Recruitment / Compliance / Patient Safety / CRO / Clinical Research Organisation

Apply for this job: Clinical Research Associate – General Medicine – Global CRO

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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