Assistant Clinical Research Coordinator

Dermatologists of Central States; Canal Winchester (OH); On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401k matching

Life insurance

Employee assistance program

Paid time off

Job summary

Dermatologists of Central States seeks an Assistant Clinical Research Coordinator to support coordination and execution of clinical trials, ensuring regulatory compliance and data integrity.

The role involves collecting data, coordinating with sponsors and sites, handling study procedures, and maintaining study documentation, with benefits including medical, dental, vision, 401k matching, and PTO.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Public Health or related field.
• Experience in clinical research preferred.
• Knowledge of GCP guidelines and regulatory requirements preferred.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint).
• Strong organizational, communication, and teamwork skills.
• Ability to work independently in a fast-paced environment.

Responsibilities

• Coordinate clinical research studies from initiation to completion.
• Collect, record, and maintain accurate study data per GCP.
• Coordinate with sponsors, trial sites, and team members.
• Perform study tasks including vital signs, ECG, and lab samples.
• Schedule visits, procedures, and tests per protocol.
• Prepare and maintain study documentation and CRFs.
• Assist with data entry, coding, and analysis as needed.
• Participate in meetings, trainings, and site visits.
• Maintain confidentiality of participant information.
• Adhere to regulations, guidelines, and policies.

Skills

Strong organizational skills

Excellent communication andinterperson

Ability to work independently and in a

Flexibility to adapt to changing pri

Education

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

Tools

Microsoft Office

Job description

Position:Assistant Clinical Research Coordinator

Location: Canal Winchester-OH-Research (OH0417), OH

Job Id:3953

# of Openings:1

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.
• 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