Data Entry Coordinator I

CenExel•Evesham Township, NJ

3d•Onsite

About The Position

Under moderate supervision, the Data Entry Coordinator I transcribes clinical research data correctly from source documents to electronic data capture following ALCOA-C principles. This role is crucial for ensuring the accuracy and integrity of clinical trial data, supporting the company's leading position in CNS and early phase studies.

Requirements

Minimum High School graduate or equivalent.
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.

Nice To Haves

One year of data entry or related preferred.

Responsibilities

Ensures timely data entry through department and study tracking.
Maintains healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well as 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.