Clinical Research Coordinator & Compliance Specialist

Yale University; New Haven (CT); On-site; USD 65,000 - 101,000; Part time

Benefits offered by this job

Yale Benefits

Job summary

Yale University seeks a part-time Coordinator 4, Research Support, to oversee clinical research activities, from start-up to regulatory submissions, ensuring protocol compliance across studies including the Mindful Kidney pilot trial.

The role requires a Bachelor’s degree and at least 3 years of related experience, with strong data management and collaboration skills across sponsors, investigators, and regulatory authorities. On-site work in New Haven, CT is expected.

Qualifications

• Bachelor’s degree in a relevant scientific field and at least 3 years of research support experience.
• Experience coordinating clinical trials and regulatory submissions is essential.
• Proven ability to manage multiple projects and adhere to timelines.

Responsibilities

• Coordinate studies and ensure protocol and funding congruence.
• Maintain regulatory documentation and assist with submissions.
• Communicate with sponsors, investigators, and regulatory bodies.
• Support data collection, management, and analysis as needed.
• Assist with budget and grant-related congruency reviews.

Skills

Clinical research coordination

Regulatory compliance

Communication

Time management

EPIC data capture

Informed consent

Education

Bachelor’s degree in science/related field

3 years of related research support experience

Tools

EPIC

REDCap

Excel

OnCore

Job description

Yale University seeks a part-time Coordinator 4, Research Support, to oversee clinical research activities, from start-up to regulatory submissions, ensuring protocol compliance across studies including the Mindful Kidney pilot trial.

The role requires a Bachelor’s degree and at least 3 years of related experience, with strong data management and collaboration skills across sponsors, investigators, and regulatory authorities. On-site work in New Haven, CT is expected.