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Job Details

Clinical Research Associate/CRA Manchester

Company: Chiltern
Location: Manchester
Reference: MLJCRANOVMB
Closing Date: 06 Dec 17
Type: Full Time
Salary (£): 30,000 - 40,000
Benefits: 25 days leave, car or car allowance, pension, LI, health benefits, gym subscription contribution

Job Summary:

Excellent Home Based Permanent CRA level opportunity - Full Time in Manchester or Greater Manchester/North West region.

Requirements:

Company officially certified by the Top Employers Institute for its exceptional employee offerings for the fourth consecutive year, and for the first time, Top European Employer
Field Based positons in the Greater Manchester/North West/M62/M6
Immunology and Dermatology
Competitive salary and benefits
Full support and a focus on development
Free access to training
Great team of people
Would suit a career CRA/SCRA who enjoys UK monitoring and lots of site contact
HOME working from day one.
Monitoring only in the North West
Permanent employment with Chiltern - seconded to a top ten pharmaceutical company
12 Months rolling contract
PAYE salary and a range of benefits

We have an excellent opportunity for a CRA to work with a top ten pharmaceutical company. This is a home based full time CRA position in and around the Manchester area.

Chiltern have enjoyed a long and partnered approach with our pharma partner and both organisations are focused on the wellbeing and career development of the individual

You would be permanently employed by Chiltern on PAYE salary and benefits, and seconded to our client (pharma partner). We offer a competitive salary, car/car allowance, pension, LI, 25 days leave (increasing to 30) and other pastoral/quality of life benefits including contributions towards health club membership.

We are looking for a dynamic CRA – an individual who enjoys the thrill of building relationships with sites, is interested in career development and appreciates the benefits of being “employed” for example, career development opportunities hand in hand with Chiltern and our client.

You will receive full support in terms of line management/pastoral care, full administrative support, and access to excellent training in both soft skills and technical advancement courses.

Working within a large cross section of therapy areas, this is a rolling and renewable contract starting as a 12 months secondment.

You would typically be monitoring around 3 days/week, sometimes more sometimes less. Sites are all very regional so travel distance is minimal but there will be multiple protocols.

IMPORTANTLY - We are looking for a CRA who has at least 12 months independent monitoring experience at hospital sites either in the UK or Ireland. You may have been doing this within an academic setting and/or within an NHS trust - that is fine, as long as you have the independent monitoring skills to include site selection, initiation, monitoring and close out.

DUTIES

Contribute to the nomination of new sites for clinical trials; analyse capability and make recommendation for trial inclusion.

Assume ambassadorial role to facilitate communication between sites and Operations to increase value proposition to investigators

Facilitate preparation and collection of site level documents during all phases of the trial; resolve problems as required

Execute site initiation and training.

Implement total site management including monitoring visits, regulatory assessment, drug supply management and resolution of site problems to ensure compliance.

Identify problems at sites; resolve issues and escalate as appropriate.

Collaborate with the clinical study manager (CSM) to ensure recruitment and execute contingency plans, as needed.

Complete preparation and generation of study monitoring reports.

Review and manage data remotely and at site; resolve technical and content issues on a continuous basis in order to achieve timely database lock targets.

Implement site close-out activities.

Skills/Knowledge Required:

Ideally you will have a life science degree and at least 12 months monitoring experience in the UK within either the Pharma or CRO setting. We will also consider monitors who have come from an academic setting or from within the NHS and have taken part in investigator led studies.

please contact Marc Joseph on 01753 216664 for further information or send your CV and application to marc.joseph@chiltern.com

key words CRA, clinical research associate, monitoring, site management


Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.

Apply for this job: Clinical Research Associate/CRA Manchester

Contact Information:

Address:  London, UK
171 Bath Road Slough Berkshire
SL1 4AA, UK
England
Tel:  +44 (0) 1753 512000
Fax:  +44 (0) 1753 511116
Website:  Visit Our Web Site

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