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Clinical Trial Associate - Turkish (Fluent) job in Cork at Bespoke Recruitment

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Clinical Trial Associate - Turkish (Fluent) at Bespoke Recruitment

Clinical Trial Associate - Turkish (Fluent)

Bespoke Recruitment Cork, IE Full Time
Required languages: Turkish (Business Fluent)
€35,000.00 - €55,000.00 / year
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Clinical Trial Associate - Turkish (Fluent)

Our client is a global leading pharmaceutical company who are searching for a Clinical Trial Associate to join a brand-new exciting project.

The Clinical Trial Capabilities Team provides clinical trial capabilities in support of clinical development. The Associate is accountable to ensure the investigator sites meet requirements to enrol study participants into clinical trials and support ongoing activities during site maintenance and closeout. The Associate is responsible for obtaining clinical trial authorizations and ethical approvals, execution of the budget and contract, and activities related to clinical finance, records management, and site training.

The Associate will ensure inspection readiness through a complete, accurate and readily available Trial Master File. Additional local responsibilities may be required as needed/appropriate for the local geography and/or to cover regional differences.


  • Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site’s ERB and Competent Authority (CA)(where applicable), communicate and negotiate budgets with site personnel and internal teams,  negotiate and obtain fully-executed contract,  track and ensure site compliance to required training, and effectively drive timelines aligned with company priorities
  • Communicate directly with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out
  • Identify, communicate, and resolve issues
  • Ensure country specific regulatory and data privacy requirements are incorporated into submission documents and any other documents/systems
  • Leverage previous site / review board engagements to efficiently drive new work
  • Populate internal systems to ensure accuracy of trial / site performance
  • Understand and comply with procurements, legal, financial requirements and procedures
  • Populate Trial Master Files and libraries for future reference
  • Provide feedback and shared learning for continuous improvement
  • Leverage trial prioritization
  • Anticipate and monitor dynamically changing priorities

Basic Qualifications
Bachelor’s degree preferably in a scientific or health related field, two years clinical research experience or relevant experience preferred
Understanding of overall clinical development paradigm and the importance of efficient site initiation
Applied knowledge of project management processes and skills
Appreciation of / experience in compliance-driven environment
Ability to learn and comply with financial and legal guidelines and policies (budget and contract)

Additional Skills/Preferences

Effective communication, negotiation, and problem-solving skills


Salary: 35-55k year + 5% bonus

*Fluent in English and Hebrew

** Due to the nature of the position, the candidate must have EU work permit or be an EU citizen

Recommended Skills

Clinical Research
Pre Clinical Development
Trial Master File
Clinical Trials
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