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CRAII/ SCRA - Turkey
- Permanent
- Clinical Research Associate (CRA)
- Turkey
This vacancy has now expired. Please see similar roles below...
Proclinical are working with a global Clinical organisation searching for a Clinical Research Associate/ Senior Clinical Research Associate for a hybrid position based in Turkey and offers the flexibility of hybrid working. The successful candidate will be significant in conducting different types of site visits, ranging from feasibility to close-out. A key part of this role is ensuring data integrity and compliance with SOPs, GCP, and other regulatory requirements.
Responsibilities:
- Conduct all site visits according to plan, document actions and follow up with action plans.
- Train and support site staff in safety information handling, systems and protocols, and trial procedures to minimize protocol deviations.
- Proactively use EDC and other data source systems for preparation and then conduct on-site visits. Also, source data verification in collaboration with the data management and the logistics team.
- Identify potential risks and proactively take action to prevent further risks in the future.
- Assist in ensuring data cleaning cycle timelines are completed in time within accordance of the Data Flow Plan.
- Build strong relations with site personnel to assist being their preferred clinical research partner.
- Complete the filing and archiving trial documentation in the Investigator Trial Master File (ITMF) for the site.
- Be involved in Investigators Meetings and be an active presentation in order to maintain relations with sites.
- Maintain knowledge of global and local SOPs, GCP, and other regulatory requirements.
- Support audits and inspections at sites and affiliate, as required.
Key Skills and Requirements:
- Bachelor or Master's degree in life sciences or another relevant field.
- Previous proven experience as a Clinical Research Associate.
- Knowledge in therapeutic areas such as oncology, diabetes, psychiatric, neurology, cardiology studies or similar is an advantage to the role.
- Outstanding knowledge of Trial Management, Clinical Trial Management Systems and Good Clinical Practices.
- Excellent analytical and communication skills within industry understanding and stakeholder management.
- Fluency in English and a full valid driver's license.
Interested or know someone who might be? Reach out to Yaseen Damasico using the following:
✉️ y.damasico@proclinical.com
Apply now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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