Clinical Research Coordinator

Clinical Research Coordinator Next Phase Research Hollywood, FL Job Details Full-time From $60,000 a year 21 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Vision insurance Qualifications Spanish Biostatistics HIPAA English Crossover clinical trial design High school diploma or GED Collecting samples for laboratory testing Data collection Factorial clinical trial design Healthcare research FDA regulations Full Job Description Job Summary The Clinical Research Coordinator (CRC) is responsible for supporting and managing the daily operations of clinical research studies within a pharmaceutical or medical research setting. This role ensures that all research activities are conducted in compliance with ICH-GCP (International Council for Harmonisation - Good Clinical Practice) guidelines, study protocols, and regulatory requirements. The ideal candidate will demonstrate strong attention to detail, data accuracy, and a commitment to upholding the highest ethical standards in human subject research. Fluency in English and Spanish is required. Experience in psychiatry or neuroscience research is preferred. Essential Responsibilities and Duties

• Coordinates all aspects of study implementation, from site initiation to study closeout, under the direction of the Principal Investigator (PI).
• Oversees subject screening, enrollment, informed consent, and ongoing study participation to ensure compliance with study protocols.
• Manages data collection, entry, and verification to maintain accuracy and data integrity across multiple studies.
• Collaborates with pharmaceutical sponsors, contract research organizations (CROs), and monitors to ensure timely communication and regulatory compliance.
• Assists in preparation, submission, and maintenance of regulatory documents, including IRB submissions, source documentation, and case report forms (CRFs).
• Tracks and reports adverse events (AEs), serious adverse events (SAEs), and protocol deviations according to sponsor and FDA requirements.
• Maintains and organizes research files, study binders, investigational product accountability logs, and essential documentation per GCP guidelines.
• Performs study-related procedures such as vital signs, EKGs, phlebotomy, and other clinical assessments per protocol.
• Participates in investigator meetings, monitor visits, and audits to ensure ongoing compliance and data quality.
• Assists with training staff and developing best practices for research and data management.
• Contributes to protocol development, feasibility assessments, and study start-up activities as needed.
• Other research-related duties as assigned by the Principal Investigator or Clinical Operations Manager.

Education / Experience

/ Skills

• Bachelor's degree in a scientific, healthcare, or research-related field (preferred).
• 1-3 years of experience in clinical research, pharmaceutical studies, or healthcare (required).
• Experience in psychiatry or neuroscience research preferred.
• Fluency in English and Spanish required.
• Working knowledge of FDA, ICH-GCP, and HIPAA regulatory guidelines governing clinical trials.
• Experience in electronic data capture (EDC) systems, such as Medidata RAVE, REDCap, or similar platforms.
• Strong organizational, time management, and documentation skills with a focus on data accuracy.
• Excellent interpersonal communication skills with patients, staff, and external partners.
• Ability to work independently and collaboratively in a fast-paced, regulated environment.

Job Type:

Full-time Pay:

From $60,000.00 per year

Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance Application Question(s): Do you have experience in the medical research or pharmaceutical industry?

Language:

Spanish (Required) Ability to

Commute:

Hollywood, FL 33024 (Required)

Work Location:

In person