Clinical Trials Research Associate II

Yale University; New Haven (CT); On-site; USD 68,000 - 121,000; Full time

Job summary

Yale University in New Haven seeks a Coordinator 4, Research Res Support, to provide professional support for large, complex multidisciplinary projects. You will oversee study start-up, recruitment, data collection, regulatory submissions, and compliance, coordinating with researchers and stakeholders to ensure timely, accurate results.

The role emphasizes training and coordinating the research team, managing patient interactions, and maintaining adherence to regulatory standards, with

Qualifications

• Experience in a research or clinical setting with clinical trials.
• Experience with patient recruitment and informed consent.
• Experience with IRB submissions and regulatory processes.
• Ability to manage multiple projects with attention to detail.
• Strong interpersonal skills for diverse stakeholders.
• Proficiency with EMR, data abstraction and trial management systems.
• Excellent organizational and time-management capabilities.

Responsibilities

• Designs and oversees complex multidisciplinary research projects from start to finish.
• Collaborates with Principal Investigator to define research goals and methods.
• Solves methodological and procedural problems through designed approaches.
• Plans supplies and equipment to ensure smooth lab operation and budgets.
• Analyzes data, evaluates data collection methods, and ensures data integrity.
• Coordinates lab renovations with Facilities, Health & Safety, and Purchasing.
• Prepares scientific reports for proposals and publications.
• May perform additional duties as assigned.

Skills

Clinical trials experience

Recruitment & consent

IRB submissions

Multi-project management

Stakeholder communication

EMR & data management

Time management

Education

Master's degree in a scientific discipline

Tools

REDCap

Electronic Medical Records systems

Job description

Yale University in New Haven seeks a Coordinator 4, Research Res Support, to provide professional support for large, complex multidisciplinary projects. You will oversee study start-up, recruitment, data collection, regulatory submissions, and compliance, coordinating with researchers and stakeholders to ensure timely, accurate results.

The role emphasizes training and coordinating the research team, managing patient interactions, and maintaining adherence to regulatory standards, with