Alimentiv
Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
201 - 500
Clinical Operations Lead
September 20
Alimentiv
Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management
201 - 500
Description
• Responsible for clinical operations oversight of projects • Provides support to CRAs and investigator sites • Develop training materials and implement recruitment strategies • Conduct regular CRA calls and provide project updates
Requirements
• Fluent in the reading, writing, and speaking of English • Undergraduate university degree (Bachelors or Honors Bachelors) AND 4-6 years' experience + substantial on-going job-related training • Should have a minimum of 3 years CRA experience, have strong experience with EDC systems, be proficient with MS Office, have strong written and verbal communication skills and highly effective interpersonal and organizational skills. • Demonstrate the following attributes: proactive, detail oriented, task-driven and highly organized. • Demonstrate the critical elements of GCPs and local regulations as they relate to clinical monitoring, IRB/EC and Investigator responsibilities. • Demonstrated ability in report writing and strong ability to critically understand clinical research documents. • Ability to handle multiple tasks to meet deadlines in a dynamic environment.
Benefits
• Health Sciences, Life Sciences or Nursing specialty preferred, or SoCRA and/or ACRP Certification/Designation. • Home-based
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