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Job Details

Clinical Project Leader

Company: Chiltern
Location: Gouda, Randstad, The Netherlands
Reference: CPLM-IdHNL
Closing Date: 31 Oct 16
Type: Contract
Salary (£): On Application

Job Summary:

The CPL is responsible for the set up and progress of a clinical trial/study within the allocated countries, ensuring compliance with company quality standards and regulations in force, the forecasted timelines, milestones and budget.


Duties & Responsibilities
• represents the countries in his/her perimeter at the global Clinical Trial Team (CTT) and is the main contact for the Regional Trial Manager (RTM) and global CTOM.
• ensures liaison with other CTT members.
• leads the monitoring teams in the designated countries for his/her trials
• represents the CSU at Medical Affairs/Business Unit meetings to feed back on study progress


• Educated to degree level in a science or medical speciality. A post graduate qualification is highly desirable.
• Minimum of 5 years of experience in clinical research
• Knowledge of clinical trial design and development in relevant therapeutic areas.
• Thorough working knowledge of all aspects of GCP and the regulatory/ethical framework pertaining to clinical trials; Ability to plan, set and manage clinical trial budgets.
• Ability to learn and apply SOPs.
• Good IT skills in, e.g. MS Office, are essential, for planning, tracking, communicating and reporting.
• Management, leadership, negotiation skills and communication skills, organizational,analytical and planning abilities, results oriented, quality preserving, be proactive and able to anticipate and resolve conflicts/issues, reactivity to emergent needs, able to prioritize, time management
• Fluent in English



Apply for this job: Clinical Project Leader

Contact Information:

Address:  Netherlands
Schipholweg 111, 2316 XC Leiden, Netherlands

Tel:  +31 71 711 2500
Website:  Visit Our Web Site

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