Clinical Research Coordinator [Bilingual]

Rovia Clinical Research

Doral, FLFull-time

50K–55K a year

Behavioral Health Market Context

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Job Description

act. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

Key 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.

Skills/Abilities:
• 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.
• Fluent in English and Spanish.

Education/Experience:
• High school diploma required, bachelor’s degree in related field preferred.
• 1 year of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.

The pay range for this role is:
50,000 - 55,000 USD per year(Doral)

Qualifications

  • 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
  • Fluent in English and Spanish
  • 1 year of clinical research experience

Benefits

  • 50,000 - 55,000 USD per year(Doral)

Responsibilities

  • The Clinical Research Coordinator (CRC) is responsible for coordinating and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs
  • This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success
  • 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


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