BA BS Required
Minimum of 1 Year Clinical Research Experience Requried
This Clinical Research Coordinator position entails a high volume of data abstraction; no patient contact. The focus of this position is Oncology Clinical Trials. At least 1 year of previous clinical research data entry experience is required.
As a direct report to the Clinical Research Project Manager this experienced Clinical Research Coordinator will assist multiple different disease group with the demanding data requirements of our actively enrolling clinical research studies.
This PartTime Clinical Research Coordiantor assists with the following for multiple studies:
Collects and interprets data necessary for enrollment; registers patients
Monitors and evaluates protocol compliance
Manages data collection via chart abstraction and submits data in timely fashion
Monitors and reports adverse events as required by institutional/federal regulations
Resolves data discrepancies as requested by Sponsors
Coordinates and processes tissue samples as required by protocol
Prepares submission of protocol revisions and safety reports to the IRB
Prepares annual progress reports for IRB renewal of ongoing studies
Participates in monitoring visits and makes data corrections as required by Monitor
This is a 2024 hour/week position. The majority of the hours will occur between 9am and 4pm though the schedule within these hours may fluctuate.
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills perspectives and ideas we choose to lead. Applications fromprotected veterans and individuals with disabilities are strongly encouraged.
Required Experience:
Chief