Clinical Research Associate

3 weeks ago


Reston, Virginia, United States Medix™ Full time

We are seeking a highly motivated Clinical Research Coordinator to join our team at Medix™. As a key member of our research team, you will be responsible for coordinating the implementation of multiple complex clinical research protocols.

Responsibilities:

  • Coordinates the implementation of multiple complex clinical research protocols.
  • Develops SOPs and templates with guidance from the PI and/or Clinical Research Manager.
  • Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
  • Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
  • Plans strategies to monitor, document, report, and follow-up on unanticipated occurrences and protocol deviations. Develops and implements preventive/corrective actions.
  • Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
  • Organizes/manages site visits and internal/external auditing activities as assigned.
  • Coordinates research team meetings; assures communications in cross-functional teams.
  • Assures synchronization of study visits/procedures/clinical tests with data collection schedules, established time-points; manages progress of study participants through protocol; expedites overall study progression.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.

Benefits:

  • Medical, Dental, Vision insurance
  • PTO and paid holidays
  • 401k with employer match
  • Mental Health Assistance, Gym Discounts, Referral Program and more


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