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Job Details

Clinical Research Associate or Senior Clinical Research Associate – Russia

Company: Chiltern
Location: St Petersburg or Moscow
Reference: SKCRA
Closing Date: 24 Jun 18
Type: Permanent
Salary (£): Negotiable
Benefits: Competitive salary and benefits

Job Summary:

• Clinical Research Associate or Senior Clinical Research Associate • St Petersburg or Moscow preferred locations • Working for Chiltern

Requirements:

Due to our continuing success and expansion, Chiltern are currently looking for experienced Clinical Research Associates to work with our team in Russia.
 
CRA/ SCRA is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The work will involve Clinical Monitoring activities for designated projects and to monitor specified sites to ensure quality and integrity of data, compliance with Chiltern International or Sponsor’s SOPs, ICH GCP, and regulatory requirements, ensuring study completion on time and within budget

Job Primary Functions:

The successful applicant will be responsible for coordinating Phase I-IV clinical trials in Europe

Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.

Assist with document submissions to local authorities

To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required

Ensure that all study related communication including e-mail is tracked, printed and filed as required

To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA

To liaise with all other appropriate departments within Chiltern International to ensure the smooth running of the study

Mentor and train other CRA’s

To assemble files and ensure documents for the trial master file accurately reflect the progress of the study

Other Ad-Hoc CRA duties

Job Qualifications:

A BSc or BA degree in a biomedical or related life science, or nursing qualification

Candidates should ideally have 2 years + CRA experience

Good clinical knowledge with an understanding of medical terminology

An understanding of the basics of physiology and pharmacology

Understanding of the principles of ICH GCP and regulatory requirements

Experience using a clinical trial management system

Preferable experience using a clinical trial management system (CPMS)

Experience as a CRA on single site and/or multicentre trials

Good oral and written communication, organizational skills and personal presentation

The ability to communicate effectively in Russian and English

Good computer literacy with working knowledge of PCs, Windows and Microsoft Office    applications

Therapeutic Focus
The successful candidate will have well rounded and recent therapeutic experience within the areas of Biopharma (mixed therapeutics)

 

Additional Information:

This is a permanent, full time role

Work will be required away from Chiltern offices, at Sponsor offices, and will require national travel

May also involve travel to meetings or attendance at conferences

Overnight stays may be required

No freelance applications

To apply for this position please send your CV to Sergei.Kozhin@covance.com or for a confidential discussion please call Sergei on +7 495 775 7310.

 

Please note that if your experience does not mirror that of our requirements for this role you may not receive a response

 

 

Apply for this job: Clinical Research Associate or Senior Clinical Research Associate – Russia

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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