Data Entry Coordinator I

CenExel•Marlton, NJ

2d•Onsite

About The Position

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process. Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k. Job Summary: Under moderate supervision, the Data Entry Coordinator I transcribes clinical research data correctly from source documents to electronic data capture following ALCOA-C principles. Compensation: $19.67-$25.21/hr depending on experience, education, and skill set

Requirements

Minimum High School graduate or equivalent.
One year of data entry or related preferred.
Must have excellent computer skills and medical/research terminology.
Must be self-directed and able to work with minimal supervision.
Motivated to work consistently in a fast paced and rapidly changing environment.
Able to manage multiple projects and responsibilities.
Must be able to effectively communicate verbally and in writing.

Responsibilities

Ensures timely data entry thru department and study tracking, etc.
Maintains healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well key clinical trial personnel.
Transcribes data accurately and efficiently from source documents to electronic data capture.
Assists in preparing for internal and external data audits along with the clinical operations/ quality/ and regulatory teams.
Completes training and obtains applicable certificates and access to CRFs/EDC.
Verifies source documents (e.g., “buddy check”).
Assists CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials.
Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
Assumes other duties and responsibilities as assigned.