Research Data Coordinator

Astera • East Brunswick, NJ

3d • Onsite

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.

Requirements

• A Bachelor’s degree or equivalent working experience required.
• Detailed oriented
• Good communication skills
• Ability to prioritize multiple projects and meet deadlines
• Excellent organizational and time management skills

Nice To Haves

• 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.

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.

Benefits

• Comprehensive benefit package
• Paid time off
• Medical, dental, vision, life, disability, HSA, FSA and other ancillary benefits
• 401(k) plan with company contribution
• Profit sharing
• Tuition assistance
• Employee referral bonus

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level