Research Data Coordinator
About The Position
You will be an integral part of clinical studies at Astera Cancer Care by primarily managing study data with supporting CRC for the successful management of clinical trials. This is a full-time position. Core Responsibilities Include: Study Data management: Enter research data into a centralized database as per protocol requirements Answer and resolve EDC queries on a timely manner Communicate with study team during monitoring visit Organize study subject folders Internal review of study documentation integrity Create and update source documents, such as case report forms Other supporting responsibilities: Patient pre-screening assigned by supervisor Assist in the coordination of tests and visits for patients and collaborate with the Astera study team to maximize work efficiency and productivity. Collaborate with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials. Confer with all members of the clinical team to confirm appropriateness and timeliness of tests. Attend investigator meetings as required or requested by the Principal Investigator. You will be an integral part of clinical studies at Astera Cancer Care by primarily managing study data with supporting CRC for the successful management of clinical trials. This is a full-time position. Core Responsibilities Include: Study Data management: Enter research data into a centralized database as per protocol requirements Answer and resolve EDC queries on a timely manner Communicate with study team during monitoring visit Organize study subject folders Internal review of study documentation integrity Create and update source documents, such as case report forms Other supporting responsibilities: Patient pre-screening assigned by supervisor Assist in the coordination of tests and visits for patients and collaborate with the Astera study team to maximize work efficiency and productivity. Collaborate with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials. Confer with all members of the clinical team to confirm appropriateness and timeliness of tests. Attend investigator meetings as required or requested by the Principal Investigator.
Requirements
- A Bachelor’s degree or equivalent working experience required.
- One (1) year of clinical research experience preferred.
- Oncology experience a plus.
- Experience with EDC, IWRS, CRF and Microsoft applications preferred.
- Experience with data management preferred.
- Detailed oriented
- Good communication skills
- Ability to prioritize multiple projects and meet deadlines
- Excellent organizational and time management skills
Responsibilities
- Enter research data into a centralized database as per protocol requirements
- Answer and resolve EDC queries on a timely manner
- Communicate with study team during monitoring visit
- Organize study subject folders
- Internal review of study documentation integrity
- Create and update source documents, such as case report forms
- Patient pre-screening assigned by supervisor
- Assist in the coordination of tests and visits for patients and collaborate with the Astera study team to maximize work efficiency and productivity.
- Collaborate with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials.
- Confer with all members of the clinical team to confirm appropriateness and timeliness of tests.
- Attend investigator meetings as required or requested by the Principal Investigator.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
