Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator

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.

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.

• 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.

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

• 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