Clinical Research Coordinator

Responsibilities

• Conducts and coordinates patient visits in accordance with study protocols
• Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable
• Ensures informed consent is properly obtained and documented
• Educates and guides participants through the study, ensuring a positive patient experience
• Monitors subject safety, reports adverse events, and escalates concerns as appropriate
• Completes timely and accurate source documentation and EDC data entry
• Resolves data queries and ensures data integrity
• Maintains investigational product accountability and proper storage and handling
• Prepares for and supports monitoring visits, audits, and inspections
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow
• Perform other duties as assigned

Preferred

• bachelor's degree in related field
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) or ophthalmology tasks (OCT imaging, measuring IOP, etc.) strongly preferred
• Rovia Clinical Research is a US-based multi-specialty clinical research site network that partners with healthcare providers.
• Hattiesburg, Mississippi, USA
• https://roviaclinical.com
• Growth Stage
• Total Funding
• unknown
• Key Investors
• Marathon Asset Management
• 2025-11-06
• Debt Financing
• Recent News
• Business Wire
• Marathon Asset Management Provides Senior Financing to Rovia Clinical Research
• 2025-11-07
• PR Newswire
• Rovia Clinical Research Announces Partnership with the Hattiesburg Clinic to Launch New Research Site in Hattiesburg, Mississippi
• 2025-10-31
• Redefining Clinical Success for Sites Through Patient-Centered Support, Upcoming Webinar Hosted by Xtalks

Qualifications

• High school diploma required
• 2+ years of clinical research experience
• Strong knowledge of medical terminology and clinical procedures
• Understanding of ICH/GCP and regulatory requirements
• Excellent organizational skills and attention to detail
• Strong interpersonal and patient-facing communication skills
• Ability to multitask and manage competing priorities in a fast-paced environment
• Proficiency in Microsoft Office, EDC, and CTMS applications
• Ability to work both independently and collaboratively
• High level of professionalism and commitment to patient confidentiality
• Bachelor's degree in related field
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) or ophthalmology tasks (OCT imaging, measuring IOP, etc.) strongly preferred

Required skills

• Clinical Procedures, Clinical Trial Management System (CTMS), Clinical Trials Management, EKG, Electronic Data Capture (EDC), ICH/GCP Guidelines, Informed Consent Documentation, Medical Terminology, Microsoft Office, OCT Imaging, Patient-facing Communication, Phlebotomy, Vital Signs Measurement

Preferred skills

• 2025-10-15, 2025-10-31, 2025-11-06, 2025-11-07, AI Tools, Analyze How Well You Fit, Build Cover Letter, Business Wire, Company data provided by, Customize Your Resume, Debt Financing, Growth Stage, Hattiesburg, Mississippi, USA, Key Investors, Make your application stand out, Marathon Asset Management, Maximize your interview chances, PR Newswire, Recent News, Total Funding, Understand your strength & weakness, bachelor's degree in related field, https://roviaclinical.com, unknown

Experience

• 2+ years