Data Coordinator 2

Overview

The Research Assistant 2 HSS supports research in clinical trials, public health, or other health service-related areas by screening and recruiting subjects for studies, conducting structured interviews, and collecting specific data in various environments according to specified sources and protocols. They provide limited data analysis; collect specimens in the field or clinic environment, or perform chart reviews to identify specific criteria for studies; participate in presentations or orientation of study participants; and conduct literature research supporting publication efforts. They are responsible for administrative tasks such as preparing budgets, ordering supplies, preparing grants, presentations, and scientific papers. The role includes working independently and within a team, with duties varying depending on the specific research project.

Required Skills and Abilities

1. Proven ability to work with research protocols and clinical trials; adept at collecting and managing data.
2. Strong interpersonal skills, excellent written and verbal communication abilities, and experience working with diverse groups or patient populations.
3. Intermediate to advanced proficiency with Microsoft Office Suite (Excel, Word), electronic medical databases, and other relevant software.
4. Excellent organizational skills, attention to detail, and the ability to manage multiple tasks and priorities efficiently in a fast-paced environment.
5. Strong customer service orientation, with the ability to handle sensitive information confidentially and professionally.

Preferred Skills and Abilities

1. Bachelor's degree in a related field such as psychology, neuroscience, or public health; experience administering structured clinical interviews or managing research studies.
2. Familiarity with research regulations, ethical guidelines, and Institutional Review Board (IRB) procedures.
3. Experience with data management software, such as REDCap, OnCore, and clinical trial management systems (CTMS).
4. Prior experience in a clinical setting, working with subjects with psychiatric or cognitive disorders.
5. Completion of Good Clinical Practice (GCP) training, with certification as a Clinical Research Associate (CRA) or Clinical Research Professional (CRP) preferred.

Principal Responsibilities

1. Researches and collects data through site or home visit intakes; library research; structured interviews; or through other means for research projects.
2. Interprets, synthesizes, and analyzes data using scientific or statistical techniques. Modifies and plans research experiments, procedures, tests, or survey instruments. Assists in research design.
3. 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.
4. Schedules and coordinates research activities. Identifies and recruits study participants. Orders and maintains inventory of supplies.
5. May assist in preparing financial information and monitoring budgets.
6. 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.

Hourly Range

$31.05

Job Details

• Job Category: Technician
• Time Type: Full time
• Work Model: Hybrid
• Location: 2 Church Street South, New Haven, Connecticut