Senior Clinical Research Associate - Sponsor Dedicated - Turkey

As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Perform all type of visits from site feasibility to close out visits according to plan, document actions and follow up on action plans
• Train and guide site staff in safety information handling, systems, protocol and trial procedures to minimize protocol deviations
• Proactive use of EDC and other data source systems for preparation and conduct on site visits as well as source data verification in collaboration with data management/logistics team
• Identify potential risks and proactively take action to prevent or mitigate
• Collaborate with Data Management/logistics in resolving queries
• Assist to ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan
• Motivate and build strong relations with site personnel to assist the sponsor in being their preferred clinical research partner
• Collaborate with and provide oversight of deliverables from vendors locally, if applicable
• Support the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF)
• Participate in Investigators Meetings to ensure relations with sites as well as active presentation as applicable
• Maintain knowledge of and act in compliance with global and local SOPs, GCP and other regulatory requirements
• Support audits and inspections at sites and affiliate, as applicable

You are:

• Bachelor or Master’s degree in life sciences or other relevant fields.
• At least 3 years of experience as a Clinical Research Associate.
• Therapeutic area knowledge and demonstrating an understanding of oncology, diabetes, psychiatric, neurology, cardiology studies or similar is an advantage.
• Excellent knowledge of Clinical Trial Management Systems, Good Clinical Practices and Trial Management.
• Strong analytical and communication skills with business, industry understanding and stakeholder management.
• Fluent in English.
• Valid driver’s license

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