Data Entry - Clinical Research

CenExel•Anaheim, CA

7d•Onsite

About The Position

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. 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.

Requirements

Minimum High School graduate or equivalent.
Excellent computer skills.
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, etc.
Maintain healthy professional relationships with Clinical Operations, Quality, Regulatory, CROs, Sponsors, etc., as well 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.