Clinical Research Coordinator - DeLand, FL

Orbis Clinical is seeking a Clinical Research Coordinator for a contract-to-hire opportunity with the potential to convert to a permanent position in DeLand, FL.

Schedule: Monday–Friday, 7:00 AM–4:00 PM ET

Location: On-site, Deland, FL

Employment Type: Contract-to-hire

Overview

An established clinical research site in Central Florida is seeking an experienced Clinical Research Coordinator to support ongoing and upcoming Phase I–III clinical trials across multiple therapeutic areas. This is a contract-to-hire opportunity for a CRC who can step into an active research environment, contribute quickly, and maintain a high standard of documentation, organization, and patient care.

Job Description

The Clinical Research Coordinator will support day-to-day clinical trial execution and serve as a key point of contact for study participant. Responsibilities include:

• Support patient pre-screening, screening, enrollment, scheduling, and follow-up
• Coordinate protocol-required visits, procedures, and study activities
• Maintain accurate source documentation and case report forms
• Support adverse event and serious adverse event documentation and reporting
• Prepare for monitoring visits, audits, investigator meetings, and study training
• Assist with patient recruitment and study logistics
• Maintain compliance with study protocols, ICH/GCP, site procedures, and applicable regulatory requirements
• Collaborate with investigators, sponsors, CROs, patients, and monitors
• Manage multiple priorities while maintaining strong attention to detail and follow-through

Requirements & Experience

• Strong understanding of ICH/GCP and clinical research requirements
• High level of attention to detail and accuracy
• Strong documentation, organizational, analytical, and data-management skills
• Ability to maintain confidentiality and appropriately handle sensitive information
• Proactive working style with strong ownership and follow-through
• Ability to manage multiple studies and competing priorities in a fast-paced environment
• Strong interpersonal and communication skills
• Phlebotomy experience or certification preferred
• Clinical background such as RN, LPN, MA, CNA, EMT, Paramedic, or similar preferred

Degree/Education Requirements:

• No specific degree required. Relevant clinical education or credentials are preferred.

Years of Experience:

• Minimum 2 years of hands-on Clinical Research Coordinator experience. Experience supporting Phase I, II, and III clinical trials is required.

Compensation Details

• Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
• The Pay Range for this position is $29.00–$34.00 per hour, can vary depending on employment status.
• Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k). 

EEO and Reasonable Accommodation Statement:

Stone Harbor Staffing Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us.

By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.