Role OverviewProvides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
What You Will Do
Creating and maintaining patient charts, preparing participant visits, maintaining inventory of study specific supplies, completing data entry and query resolution, communicating with study participants, and assisting Coordinators with scheduling and other clerical tasks.
Why It Might Be a Fit
Strong personal initiative, attention to detail, ability to react calmly in emergency situations, and ability to clearly communicate both orally and verbally.
Requirements
- California Medical Assistant Certification
- Interest in and knowledge of specific study indications
- Excellent computer skills
- Advanced knowledge of electronic equipment
- Skilled in organization and record maintenance
- Skilled in developing and maintaining effective working relationships
- Strong personal initiative
- Attention to detail
- Ability to react calmly in emergency situations
- Ability to clearly communicate both orally and verbally
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