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Job Details

Clinical Research Associate II (CRA II) - UK

Company: PAREXEL
Location: Uxbridge
Reference: 39754BR
Closing Date: 13 Dec 17
Type: Permanent
Salary (£): Competitive
Benefits: Competitive Corporate Benefits including company car or car allowance, CRA incentive bonus, holiday, pension, life assurance and more.

Job Summary:

Clinical Research Associate II / CRA II / UK / Uxbridge / monitoring / onsite / remote / clinical trials / visits


PAREXEL strives to be the premier provider to the biopharmaceutical and medical device industries for the development and commercialization of new medical therapies worldwide. Our mission is to combine the strength of our expertise, experience and innovation to advance the worldwide success of the biopharmaceutical and medical device industries in preventing and curing disease.

We believe that PAREXEL provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities.

This role can be either based at our UK Head Office situated in Uxbridge, this is close to both Uxbridge train station as well as the town centre and the building has plenty of free parking or it can be home based when you are not required to be at site.

Your Key Accountabilities:

- Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
- Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
- Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
- Build strong working relationships with investigators and site staff
- Manage clinical monitoring activities, including:
    + Arranging on-site visits and logistics
    +Establishment of a site recruitment plan in collaboration with site staff during QV
    + Monitoring completeness and quality of Regulatory Documentation
    + Performing site documentation verification
    + Data collection and drug accountability in accordance with ICH GCP guideline
    + Monitoring patient safety on-site and addressing any violations in a timely manner

- Educated to degree level (biological science, pharmacy, or other health-related discipline preferred),  equivalent nursing qualification or other equivalent experience

Language Skills:
- Advanced written and oral English and fluent in relevant local language

Work Experience:
- Previous Monitoring experience (either onsite or remote) or equal clinical operations experience is preferred, however other previous clinical research in a similar environment would also be considered.

Our Offer:

We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research.

You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.

In return we will be able to offer you a structured career pathway and development within the role including awareness and understanding of the industry. Your hard work will be rewarded with a competitive base salary, company car or car allowance plus a great CRA incentive scheme as well as a benefits package including 25 days holiday per year, strong contributory pension scheme, life assurance, long term disability insurance, private medical and dental cover as well as other leading edge benefits that you would expect with a company of this type.

If you are ready to join PAREXEL’s Journey, please apply!

f this role is not for you but you are interested in working  at PAREXEL please contact or take a look under our careers page at

Apply for this job: Clinical Research Associate II (CRA II) - UK

Contact Information:

Address:  PAREXEL International
The Quays
101-105 Oxford Road
Tel:  +44 1895 238000
Fax:  +44 1895 238494
Website:  Visit Our Web Site

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