Clinical Research Specialist supporting medical innovations through study management and evidence generation. Collaborating with various stakeholders in clinical research.
Responsibilities
Performing study start-up and conducting activities that meet regulatory requirements
Identifying and investigating discrepancies in study documentation
Conducting in-house and site reviews of associated documentation
Partnering with cross-functional teams with query management, data reviews and resolution
Requirements
Bachelor's Degree in Life Sciences or Nursing
3 years of experience in clinical research (site management, clinical project management, monitoring, and/or CRC)
Experience in electronic data capture
Benefits
Competitive salaries
Performance-based incentives
A wide variety of benefits programs to address diverse individual needs
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