Clinical Research Assistant Coordinator — Trials & Data

Dermatologists of Central States; Canal Winchester (OH); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k matching

Company paid life insurance

Employee assistance program

Paid time off

Job summary

DOCS Dermatology Group seeks an Assistant Clinical Research Coordinator to support our clinical trials in Canal Winchester, OH. The role involves coordinating studies from initiation to completion, ensuring data integrity and regulatory compliance, and collaborating with sponsors and sites to maintain trial timelines.

Responsibilities include data collection, visit scheduling, and documentation maintenance, with emphasis on accuracy, confidentiality, and adherence to GCP guidelines.

Qualifications

• Bachelor's degree in Life Sciences, Nursing or Public Health, or related field.
• Experience in clinical research preferred.
• GCP familiarity and regulatory knowledge preferred.
• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills.
• Ability to work independently and in a team in a fast-paced environment.

Responsibilities

• Coordinate clinical research studies from initiation to completion.
• Collect, record, and maintain research data per GCP guidelines.
• Coordinate with sponsors, sites, and research team members.
• Perform study-related tasks including vital signs, ECG, and lab samples.
• Schedule visits, procedures, and tests per protocol.
• Prepare and maintain study documentation and CRFs.

Skills

Organizational skills

Communication skills

Independence

Attention to detail

Teamwork

Regulatory knowledge

Education

Bachelor's degree in Life Sciences / Nursing / Public Health

Tools

Microsoft Office

Job description

DOCS Dermatology Group seeks an Assistant Clinical Research Coordinator to support our clinical trials in Canal Winchester, OH. The role involves coordinating studies from initiation to completion, ensuring data integrity and regulatory compliance, and collaborating with sponsors and sites to maintain trial timelines.

Responsibilities include data collection, visit scheduling, and documentation maintenance, with emphasis on accuracy, confidentiality, and adherence to GCP guidelines.