- University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution
- In lieu of the above requirement, candidates with five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered
Minimum of four (4) years of relevant clinical research experience in a pharmaceutical company/CRO.
In lieu of the above requirements, candidates with >five (5) years supervisory experience in a health care setting and four (4) years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered
Local project coordination and/or project management experience
On the Job Experience:
Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access and Power Point)
Ability to work with minimal supervision
Excellent verbal and written communication skills
Ability to set clear expectations for junior staff on projects
Ability to resolve project-related problems and prioritizes workload for self and team
Demonstrated organizational skills and the ability to prioritize multi-tasks
Ability to understand and work with financial information
Basic knowledge of project management processes
Demonstrated ability to work within a matrix system
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