Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Clinical Site Monitor (CRA) - Turkey

Company: inVentiv Health Clinical
Location: Istanbul (Europe)
Reference: SL - Turk1
Closing Date: 16 Dec 16
Type: Permanent
Salary (£): Negotiable
Benefits:

Top Job

Job Summary:

Are you an experienced CRA in Turkey looking to work with a global Pharma?

Requirements:

Clinical Site Monitor / Clinical Research Associate (CRA) - Turkey
Office-based - Istanbul
Full-time

inVentiv Health -Transforming Promising Ideas into Commercial Reality

Job description

inVentiv Health Clinical are currently recruiting for a dedicated and motivated CRA with previous clinical research experience in Turkey to work as a Clinical Research Associate / Clinical Site Monitor. Working from the office in Istanbul you will be working on studies for a global Pharma client, playing an integral role within an established clinical research team.

You will be responsible for monitoring studies across Turkey. You will be working mainly on Phase II and III studies in various therapeutic areas including oncology.

Responsibilities will include -

Identifies new potential investigators, through collaborations with medical monitors, field personnel. Assess potential Investigators and their sites. Document and communicate visits, and provide feedback on Potential Site Assessment findings to collaborators.
Expedites the pre-study and study initiation process. Orients and trains site personnel on the study protocol, processes and regulatory requirements.
Responsible for reviewing site activities and monitoring clinical trials ensuring data quality according to relevant monitoring plans and SOPs.
Monitoring multiple protocols across multiple therapeutic areas.
Interact and build professional relationships with all study personnel at site in addition to the office based project team, handling queries and working with study team on more complex matters.
Prepares and submit written reports in a timely, accurate, concise and tactful manner.
To develop expertise in documentation requirement for ethical and regulatory submission.

Seeks and identifies potential new clinical study sites within geographical area.
Exhibits high degree of flexibility when facing changes in priorities, study modifications and enrollment changes.
Participates in team divisional, departmental meetings. Actively engages in special projects, cross functional work groups and task forces.

Eligibility/Qualifications/Requirements

To be eligible for consideration, you will come with a Life Science Degree and experience working as a Clinical Research Associate, monitoring clinical studies in Turkey (at least 2 years). You will be motivated and organized and should have excellent interpersonal and communication skills. Fluent Turkish is required in addition to English (verbal and written).

Application Details
If you have the required experience for this position and are eligible to work in Turkey then please apply or contact Stephen Larkin on +44 1628 587 275.

To find out more about our company and search and apply for other open jobs please visit our website http://www.inVentivHealthclinical.com

Apply for this job: Clinical Site Monitor (CRA) - Turkey

Contact Information:

Address:  Main Office
Thames House, 17-19 Marlow Road Maidenhead, Berkshire
SL6 7AA, UK
England
Reasons to work for inVentiv Health Clinical
Tel:  +44 (0) 1628 408 408
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.