Clinical Research Coordinator
Aviso de fuente externaen BMA Group Global
BMA Group Global seeks a Clinical Research Coordinator to coordinate study visits, maintain research data and documentation, and support protocol compliance.
Salario
No especificado
Ubicación
San Juan, Puerto Rico
Tipo de empleo
Tiempo completo
Modalidad
No especificado
Clinical Research Coordinator
San Juan, Puerto Rico
Descripción del empleo
About the role
BMA Group Global is seeking a Clinical Research Coordinator to support the day-to-day execution of clinical research studies. The role coordinates participant visits, maintains study documentation and data, and ensures research activities follow study protocols, Good Clinical Practice (GCP), and applicable regulations.
Responsibilities
- Coordinate participant visits, including screening, enrollment, and follow-up.
- Support participant recruitment and the informed consent process.
- Schedule study visits, procedures, and protocol-required activities.
- Collect and maintain accurate study data, source documentation, and electronic records.
- Enter data into study systems and address data queries as needed.
- Monitor and report adverse events and participant safety concerns.
- Maintain regulatory documents and study files.
- Ensure compliance with study protocols, GCP, and applicable regulations.
- Collaborate with investigators, sponsors, monitors, and research staff.
- Support monitoring visits, audits, and other study activities as needed.
Requirements
- Bachelor’s degree in Nursing, Life Sciences, Health Sciences, or a related field.
- Minimum of 2 years of clinical research, healthcare, or related experience.
- Strong organizational skills and attention to detail.
- Excellent communication and interpersonal skills.
- Ability to manage multiple priorities in a fast-paced environment.
- Bilingual in English and Spanish.
Preferred qualifications
- Previous experience as a Clinical Research Coordinator.
- Knowledge of GCP and clinical research regulations.
- Experience with EDC systems, study documentation, and research protocols.
Datos clave
- Requires a bachelor’s degree in Nursing, Life Sciences, Health Sciences, or a related field.
- Requires a minimum of 2 years of clinical research, healthcare, or related experience.
- Bilingual in English and Spanish.
Preguntas frecuentes
What does the Clinical Research Coordinator do?
The role coordinates participant visits, maintains study documentation and data, and supports the day-to-day execution of clinical research studies.
What are the requirements for this role?
A bachelor’s degree in Nursing, Life Sciences, Health Sciences, or a related field and a minimum of 2 years of clinical research, healthcare, or related experience are required. The role also requires bilingual English and Spanish.
What preferred qualifications are listed?
Preferred qualifications include previous experience as a Clinical Research Coordinator, knowledge of GCP and clinical research regulations, and experience with EDC systems, study documentation, and research protocols.