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Czech/Slovak native speakers - Clinical Trials Associate

Our client, a multinational pharmaceutical company, is now looking for a Czech/Slovak native speaker to join their Clinical Trials dept. as a Clinical Trials Associate.


* Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, communicate and negotiate budgets, 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 and 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


* Bachelor’s degree preferably in a scientific or health related field, two years clinical research experience or relevant experience preferred

* Understanding of the overall clinical development paradigm and the importance of efficient site activation

* 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)

* Effective communication, negotiation, and problem solving skills

* Self-management and organizational skills

* Czech/Slovak native speakers
Ireland, IE