Medix
Clinical Research Coordinator
Medix, Hyannis, Massachusetts, us, 02601
We are looking for a self-starter to join our team as a
Clinical Research Coordinator
in
Massachusetts.
We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. As a
CRC
with our esteemed organization, you will be at the forefront of cutting-edgeresearch that can positively impact patient outcomes. Join us in our mission to advance medical knowledge and make a difference in the lives of patients in
Cape Cod
and beyond.RESPONSIBILITIES1. Coordinates the implementation of multiple complex clinical research protocols.2. Develops SOPs and templates with guidance from the PI and/or Clinical Research Manager.3. Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.4. Perform blood draws and manage sample processing, packing, and shipping according to protocol, applicable standards, and regulations.5. Plans strategies to monitor, document, report, and follow-up on unanticipated occurrencesand protocol deviations. Develops and implements preventive/corrective actions.6. Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.7. Organizes/manages site visits and internal/external auditing activities as assigned.8. Coordinates research team meetings; assures communications in cross functional teams.9. 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.10. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.DETAILSMedical, Dental, Vision insurancePTO, 401k, etcWeekly pay!Monday - Friday 8a-5pMust have
experience performing phlebotomy2+ years
of experience working as a CRC
Clinical Research Coordinator
in
Massachusetts.
We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. As a
CRC
with our esteemed organization, you will be at the forefront of cutting-edgeresearch that can positively impact patient outcomes. Join us in our mission to advance medical knowledge and make a difference in the lives of patients in
Cape Cod
and beyond.RESPONSIBILITIES1. Coordinates the implementation of multiple complex clinical research protocols.2. Develops SOPs and templates with guidance from the PI and/or Clinical Research Manager.3. Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.4. Perform blood draws and manage sample processing, packing, and shipping according to protocol, applicable standards, and regulations.5. Plans strategies to monitor, document, report, and follow-up on unanticipated occurrencesand protocol deviations. Develops and implements preventive/corrective actions.6. Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.7. Organizes/manages site visits and internal/external auditing activities as assigned.8. Coordinates research team meetings; assures communications in cross functional teams.9. 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.10. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.DETAILSMedical, Dental, Vision insurancePTO, 401k, etcWeekly pay!Monday - Friday 8a-5pMust have
experience performing phlebotomy2+ years
of experience working as a CRC