Assistant Clinical Research Coordinator

Company Overview

At DOCS Dermatology Group, we are not just one of the largest dermatology practices in the nation; we are a dedicated community passionate about skin health! With more than 200 providers across 20 practice brands and 100+ locations in 10 states, we’ve been transforming the lives of our patients for more than 40 years. Our mission is clear: to prioritize our patients with outstanding medical, surgical, and cosmetic dermatology services, all delivered in a friendly, convenient, and compassionate environment.

Summary

The Research Assistant will assist in the coordination and execution of clinical trials, ensuring compliance with regulatory requirements and maintaining the integrity of research data.

Job Responsibilities

• Assist in the coordination of clinical research studies from initiation to completion.
• Collect, record, and maintain accurate and complete research data in accordance with Good Clinical Practice (GCP) guidelines.
• Coordinate with study sponsors, clinical trial sites, and other research team members.
• Complete study-related tasks including vital signs, ECG, and collecting and processing laboratory samples.
• Schedule and coordinate study visits, procedures, and laboratory tests as required by the protocol.
• Assist in the preparation and maintenance of study-related documentation, including study binders, case report forms (CRFs), and study logs.
• Assist with data entry, coding, and analysis as needed.
• Participate in study meetings, trainings, and site visits as required.
• Maintain strict confidentiality of participant information and research data.
• Adhere to all applicable regulations, guidelines, and institutional policies governing clinical research.

Benefits

• Our benefits package includes medical, dental, and vision insurance, 401k matching, company paid life insurance, employee assistance program, and paid time off.

Minimum Qualifications

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Nursing, Public Health).
• Previous experience in clinical research preferred.
• Experience with phlebotomy/venipuncture preferred.
• Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements preferred.
• Strong organizational skills and attention to detail.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
• Flexibility to adapt to changing priorities and timelines.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status