Company: inVentiv Health Clinical
Location: Istanbul (Europe)
Reference: SL - Turk1
Closing Date: 16 Dec 16
Salary (£): Negotiable
Are you an experienced CRA in Turkey looking to work with a global Pharma?
Clinical Site Monitor / Clinical Research Associate (CRA) - Turkey
Office-based - Istanbul
inVentiv Health -Transforming Promising Ideas into Commercial Reality
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.
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).
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
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