For us, what matters most is excellence. We are caring professionals, people who live, work and dedicate themselves to the communities within New Jersey and Pennsylvania. As such, we strive to provide a sanctuary of excellence, precision, thoroughness and genuine compassion. We also take a whole-person approach to patient care and treatment, tailoring all that we do around their unique needs. And we do all we can for patients, going the extra mile to see that they’re supported, informed and getting the one-on-one care and service they deserve.
Job Description:
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.
Qualifications:
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.
Competencies:
Detailed oriented
Good communication skills
Ability to prioritize multiple projects and meet deadlines
Excellent organizational and time management skills