Basic understanding of clinical study processes, with specialized technical
skills to deliver own work within the clinical study team. Ability to work
semi-autonomously with strong organizational, prioritization and analytical
Liaises with other functional areas on study-related processes.
Effectively manages time to meet project deliverables and deadlines in a manner that minimizes rework.
Takes appropriate care to ensure quality of data.
Keeps team and supervisor informed and up-to-date on information directly related to own position in the clinical operations study team.
Minimum of college degree in a relevant discipline.
Bachelor's degree in relevant scientific discipline preferred.
Must possess strong Microsoft Excel and other computer skills.
Experience in Oncology preferred.
Minimum of 3 years in Pharmaceutical Company with relevant experience.
General knowledge of basics of clinical operations.
- Familiarity and experience with Regulatory Documents/TMF
- support with study team meeting minutes
- strong organizational skills
- ability to multi-task
- possible experience with assisting with invoice processing/budgetary support (not oversight)
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