Data Coordinator - 257098

Public - Responsibilities

The Data Coordinator will provide office with direct

clinical and data management support related to the conduct of clinical trials and the

collection and reporting of study-related clinical data for clinical studies within the

assigned disease team or area. Using independent judgment and high-level decision-

making, this position is responsible for data entry, monitoring visits, and patient

scheduling for assigned disease team trials.

Public - Required Skills

Required Education and Experience Two years of related work experience in the

same job family and a Bachelore's degree in a related field; or an equivalent combination

of experience and education.

Required Skills and Abilities

1. Intermediate to advanced computer proficiency with Excel, Word and ability to utilize

electronic medical databases.

2. Ability to coordinate patient/study participant care from the recruitment phase through

off treatment and follow up phase. This coordination may require the scheduling and

verification of appointments.

3. Ability to independently and accurately abstract, create, and maintain a study

participant’s research record ensuring all required data is collected, source verified, and

entered into sponsor databases.

4. Impeccable interpersonal skills and the ability to work as a team as well as

independently while self-motivating. Professional appearance and manner as well as an

excellent attendance record. Experience working with study sponsor personnel a plus.

5. Proven ability to multitask, maintain confidentiality and manage a broad variety of

duties and shifting priorities in a changing environment and to be organized and

meticulous with details.

Public - Preferred Skills

Preferred Education, Experience and Skills

Experience coordinating, planning or working in a high-volume multi-task setting.

Knowledge of Oracle software, Medidata Rave, EPIC and ONCORE. Knowledge of

federal regulations for HIPAA and IRB. Experience working in a Clinical Trials setting

preferred. Oncology experience. Completion of Good Clinical Practice (GCP) training.