Remote Clinical Study Coordinator I — Impactful Trials

Care Access; United States; Remote; USD 75,000 - 95,000; Full time

Benefits offered by this job

Employer paid medical, dental, and vision insurance

401(k) Retirement Plan with Company Match

Paid Time Off (PTO)

Job summary

Care Access is seeking a Central Study Coordinator to manage clinical trials effectively. This remote role involves working closely with patients and study sites to ensure high-quality study delivery.

Responsibilities include conducting informed consent processes, managing participant visits, and maintaining study documentation in compliance with regulations. A Bachelor’s degree and relevant clinical research experience are required.

The expected pay range is $75,000 - $95,000 USD yearly, and the position offers extensive benefits and an inclusive work environment.

Qualifications

• At least 3 years of relevant clinical research experience.
• Experience with oncology required.
• Able to manage multiple unique protocols.

Responsibilities

• Perform informed consent procedures with study participants.
• Manage daily workflows and study compliance.
• Coordinate and facilitate participant visits.

Skills

Communication Skills

Critical Thinking

Organizational Skills

Customer Service

Problem Solving

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Office Suite

Clinical Trial Software

Job description

Care Access is seeking a Central Study Coordinator to manage clinical trials effectively. This remote role involves working closely with patients and study sites to ensure high-quality study delivery.

Responsibilities include conducting informed consent processes, managing participant visits, and maintaining study documentation in compliance with regulations. A Bachelor’s degree and relevant clinical research experience are required.

The expected pay range is $75,000 - $95,000 USD yearly, and the position offers extensive benefits and an inclusive work environment.