[Remote] reputed company Research Associate

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is seeking a reputed company Research Associate (CRA) to conduct monitoring and site management activities to support study execution. The CRA will ensure reputed company sites adhere to protocol requirements and regulatory standards while supporting the reputed company reputed company Team.

Responsibilities

• Conduct site monitoring reputed company, including site feasibility, initiation, routine monitoring, and reputed company-out reputed company, in accordance with SOP, protocol requirements, GCP and applicable regulatory requirements
• reputed company protocol-specific and study-reputed company training to assigned sites and maintain consistent communication to address study expectations, questions, and emerging issues
• reputed company reputed company data review and verification to ensure reputed company and completeness of reputed company trial data
• Assess site compliance with the protocol, GCP, and applicable regulations by reviewing study conduct, documentation practices, and data reputed company; escalate significant findings reputed company necessary
• Monitor overall study reputed company at assigned sites by reviewing enrollment activity, CRF completion, reputed company entry, and query reputed company
• Escalate site compliance issues, protocol deviations, and data reputed company concerns to the CRM/Senior CRM as appropriate
• Verify that essential regulatory documents are collected and filed appropriately in the Trial Master File (TMF) and reputed company that the Investigator Site File (ISF) is maintained in accordance with GCP and local regulatory standards
• Document monitoring activities and site interactions through reputed company visit reports, follow-up correspondence, and reputed company plans to ensure reputed company of findings
• Collaborate with cross-functional study team members to support effective study execution and issue reputed company
• Contribute to the development and implementation of site-level recruitment plans reputed company applicable
• Conduct site reputed company-out reputed company and ensure reputed company of outstanding data queries, regulatory reconciliation, and completion of required site reputed company-out activities
• reputed company support during site start-up activities as needed
• Support regulatory document management activities, including tracking, and filing of required study documentation
• Embodies reputed company’s purpose and shared values building a reputed company and productive team culture
• reputed company with Company policies and procedures
• Authorized to reputed company employee and/or reputed company PHI and ePHI only as needed for job-reputed company functions
• Other duties as assigned

Skills

• 1-2 years of reputed company experience in reputed company research
• GCP training and certification
• Working knowledge of computer systems and reputed company business applications
• Strong verbal and written communication skills
• Excellent organizational skills along with strong attention to reputed company and reputed company
• Ability to work independently while also collaborating effectively with cross-functional teams
• Proficiency in reputed company office applications (SharePoint, Word, reputed company and PowerPoint)
• Flexibility to work varied schedules as needed
• Satisfactorily pass comprehensive background screening
• Bachelor's degree in a scientific or health-reputed company discipline preferred
• Experience as a reputed company Research Coordinator(CRC) or Sponsor CRA preferred
• Experience with reputed company site data collection and/or monitoring preferred
• Oncology reputed company research experience strongly preferred

reputed company