Data Entry - Clinical Research

CenExel•Anaheim, CA

7d•$20 - $21•Onsite

About The Position

This role involves transcribing clinical research data accurately from source documents into electronic data capture systems, adhering to ALCOA-C principles. The position is within CenExel's research sites, which specialize in various phases of clinical trials across multiple therapeutic areas. The company emphasizes quality people, teamwork, and experienced management, offering a positive work environment with a good work-life balance.

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.

Nice To Haves

One year of data entry or related preferred.

Responsibilities

Comply with current protocols, SOPs, GCPs, IRB, FDA guidelines, and site training program.
Ensure timely data entry through department and study tracking.
Maintain healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well as key clinical trial personnel.
Transcribe data correctly and efficiently from source documents to electronic data capture.
Assist in preparing for internal and external data audits along with the clinical operations/ quality/ and regulatory teams.
Complete training and obtains applicable certificates and access to CRFs/EDC.
Verification of source documents (e.g., “buddy check”).
Assist CRCs in entering data from paper source documents to eCRFs correctly, accurately and on a timely manner for multiple clinical trials.
Assumes other duties and responsibilities as assigned.