Data Coordinator 2

Yale University; New Haven (CT); Hybrid; USD 43,000 - 51,000; Full time

Job summary

Yale Cancer Center is seeking a Clinical Research Assistant in New Haven to provide direct clinical and data management support for clinical trials. You will coordinate patient care from recruitment through follow‑up, abstract and verify data for sponsor reporting, and assist in trial documentation.

Working within the Yale Cancer Center/Clinical Trials Office, you’ll use Excel and EMR/database tools in a regulated, high‑volume research setting.

Qualifications

• Proficient Excel and Word; EMR/database use.
• Coordinate patient/study participant care from recruitment through follow-up.
• Ability to abstract and maintain a study data repository with source verification.
• Experience with research data reporting and documentation.

Responsibilities

• Researches and collects data through site or home visit intakes; library research; structured interviews; or other means.
• Interprets, synthesizes, and analyzes data using scientific or statistical techniques; assists in research design.
• Writes and edits material for publication and presentation; reports on status of research activities.
• Schedules and coordinates research activities; identifies and recruits study participants; orders and maintains supplies.
• May assist in preparing financial information and monitoring budgets.
• Performs additional functions incidental to research activities.

Skills

Excel

Data abstraction

Coordination of patient care

Team collaboration

Attention to detail

Education

Bachelor's degree in related field

Two years related work experience

Tools

Oracle

Medidata Rave

EPIC

ONCORE

Job description

Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community, eligible for opportunities through the New Haven Hiring Initiative, or a newcomer, interested in exploring all that Yale has to offer, your talents and contributions are welcome. Discover your opportunities at Yale!

Salary Range

$31.83

Overview

Yale Cancer Center is Connecticut's only cancer center designated as a Comprehensive Cancer Center by the National Cancer Institute (NCI). Yale Cancer Center delivers the highest quality patient-centered care, achieves breakthrough discoveries, and trains the future leaders in cancer science and medicine. There are over 300 open and enrolling trials and over 600 open trials, providing the most advanced cancer therapies at Smilow Cancer Hospital and in the 15 Care Centers, and trials are available within 20+ disease units. Yale has been at the forefront of understanding the fundamental mechanisms of cancer biology and in developing effective therapies for the treatment of cancer and harnesses the resources of the Yale School of Medicine and Smilow Cancer Hospital at Yale-New Haven to advance cancer research, prevention, and patient care, as well as community outreach and education. The Clinical Research Assistant (CRA) will provide Yale Cancer Center/Clinical Trials 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. Through the use of independent judgment and high-level decision‑making, extract, record, and disseminate treatment‑related information for regular reporting and monitoring by the research team and study sponsors.

Required Skills and Abilities

• 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. This coordination may require the scheduling and verification of appointments.
• 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. Experience working with study sponsor personnel a plus.
• 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.

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.

Principal 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.

Required Education and Experience

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.

Job Category

Technician

Bargaining Unit

L34

Compensation Grade

Labor Grade D

Time Type

Full time

Duration Type

Staff

Work Model

Hybrid

Location

300 George Street, New Haven, Connecticut

Background Check Requirements

All candidates for employment will be subject to pre-employment background screening for this position, which may include motor vehicle, DOT certification, drug testing and credit checks basedon the position description and job requirements. All offers are contingent upon the successful completion of the background check. For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.

Health Requirements

Certain positions have associated health requirements based on specific job responsibilities. These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.

Posting Disclaimer

The intent of this job description is to provide a representative summary of the essential functions that will be required of the position and should not be construed as a declaration of specific dutiesand responsibilities of the position. Employees will be assigned specific job‑related duties throughtheir hiring department. University policy is committed to affirmative action under law in employment of women, minority group members, individuals with disabilities, and protected veterans. Additionally, in accordance with Yale's Policy Against Discrimination and Harassment, and as delineated by federal and Connecticut law, Yale does not discriminate in admissions, educational programs, or employment against any individual on account of that individual's sex, sexual orientation, gender identity or expression, race, color, national or ethnic origin, religion, age, disability, status as a special disabled veteran, veteran of the Vietnam era or other covered veteran. Inquiries concerning Yale's Policy Against Discrimination and Harassment may be referred to the Office of Institutional Equity and Accessibility (OIEA).

Note

Yale University is a tobacco-free campus.