Data Coordinator 2

Yale Cancer Center conducts comprehensive cancer research, clinical trials, patient care, and education. The Data Coordinator 2 provides clinical and data management support for clinical trials by collecting, analyzing, maintaining, and reporting study-related data, coordinating research activities, and supporting participant recruitment and research staff.

Responsibilities

• Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for research projects
• Interprets, synthesizes, and analyzes data using scientific or statistical techniques. Modifies and plans research experiments, procedures, tests, or survey instruments. Assists in research design
• Writes and edits material for publication and presentation. Reports on status of research activities. Oversees and instructs research and support staff on technical procedures, equipment operation, and laboratory maintenance
• Schedules and coordinates research activities. Identifies and recruits study participants. Orders and maintains inventory of supplies
• May assist in preparing financial information and monitoring budgets
• Performs additional functions incidental to research activities

Preferred

• Experience working with study sponsor personnel a plus
• 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
• Oracle
• Medidata Rave
• EPIC
• ONCORE
• HIPAA Regulations
• IRB Regulations
• Clinical Trials
• Oncology
• Clinical Practice (GCP) Training
• Coordination
• Planning
• Sponsor Collaboration

Benefits

• Hybrid work model

Company

• Research university focused on education and knowledge advancement
• New Haven, Connecticut, USA
• https://www.yale.edu/
• Founded in 1701
• 10001+ employees

Qualifications

• Intermediate to advanced computer proficiency with Excel, Word and ability to utilize electronic medical databases
• Ability to coordinate patient/study participant care from the recruitment phase through off treatment and follow up phase
• 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
• 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
• 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
• Two years of related work experience in the same job family and a Bachelor's degree in a related field; or an equivalent combination of experience and education
• Experience working with study sponsor personnel a plus
• 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
• Two years of related work experience in the same job family and a Bachelor's degree in a related field; or an equivalent combination of experience and education.

Required skills

• Clinical Data Abstraction, Clinical Practice (GCP), Clinical Trials, Epic, HIPAA, Institutional Review Board (IRB) Compliance, Medidata Rave, Microsoft Excel, Microsoft Word, OnCore, Oncology, Oracle, Patient/Study Participant Care Coordination

Preferred skills

• Completion of Good Clinical Practice (GCP) training, Experience working in a Clinical Trials setting preferred, Experience working with study sponsor personnel a plus, Knowledge of Oracle software, Medidata Rave, EPIC and ONCORE, Knowledge of federal regulations for HIPAA and IRB, Oncology experience

Experience

• 2+ years