Data Coordinator - 257098 at Medix Data Coordinator - 257098 at Medix in East Haven, Connecticut Posted in about 5 hours ago.

Type:

full-time

Job Description:

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.