Covance

Sr Clin Res Assoc I

Job Number
2021-64512
Telecommute
No

Education/Qualifications

Minimum Required:
• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
• In lieu of the above education requirement, candidates with a minimum of 6 years recent clinical monitoring experience will be considered.
• Thorough knowledge of regulatory requirements
• Thorough understanding of the drug development process
• Fluent in local office language and in English, both written and verbal
• Or an equivalent combination of education and experience to successfully perform the key responsibilities of the job
Preferred:
• Thorough knowledge of company SOPs regarding site monitoring

Experience

Minimum Required:
• Two (2) years of Clinical Monitoring experience
• Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Advanced site monitoring skills
• Advanced study site management skills
• Advanced registry administration skills
• Ability to work with minimal supervision
• Good planning and organization skills
• Good computer skills with good working knowledge of a range of computer packages
• Advanced verbal and written communication skills
• Ability to train and supervise junior staff
• Ability to resolve project-related problems and prioritizes workload for self and team
• Ability to work within a project team
• Works efficiently and effectively in a matrix environment
• Valid Driver's License
Preferred:
• One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred
• Local project coordination and/or project management experience

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