Medical Research Cooe4rd at LA COLONIA GROUP

Miami, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

26 Jun, 26

Salary

0.0

Posted On

28 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, Patient Screening, Patient Recruitment, Enrollment, Follow-up, Documentation, Case Report Forms, Regulatory Binders, IRB, FDA, HIPAA, Data Integrity, Medical Terminology, Diplomatic Skills, Communication, Organizational Skills

Industry

Hospitals and Health Care

Description

Description POSITION SUMMARY: Clinical research center is seeking a highly motivated and detail-oriented Medical Research Coordinator to join our team. This role is crucial in supporting and managing clinical research studies, ensuring compliance with all regulatory guidelines (IRB, FDA, HIPAA), and contributing to the advancement of patient care through evidence-based practice. DUTIES & RESPONSIBILITIES: Responsibilities include but are not limited to: • Coordinate the daily activities of clinical research studies, including patient screening, recruitment, enrollment, and follow-up. • Maintain accurate and complete study documentation, case report forms (CRFs), and regulatory binders. • Ensure all research activities comply with the study protocol, institutional policies, and all applicable federal and local regulations. • Serve as the primary liaison between investigators, internal departments, and external research sponsors. • Manage and process clinical samples, collect and enter research data, and ensure data integrity and security. • Assist in the preparation and submission of new protocol applications, amendments, and renewal reports to the Institutional Review Board (IRB). • Conduct patient interviews and administer questionnaires as required by the study protocol. • Maintain a clean and orderly work area and patient rooms. • Complete quality control activities, monitor equipment operation, and report any equipment malfunctions to the supervisor. • Process medical documentation for visits and follow up with patients as needed. • Adhere to all company safety policies and procedures and immediately report any anomalies following established guidelines. • Perform other duties as assigned. Requirements QUALIFICATIONS: • High school diploma or equivalent. • Medical Assistant (MA) license or certification is required. • Minimum of 2 years of experience in clinical research coordination or a related role. • Proficiency with medical terminology and clinical procedures. • High school diploma or equivalent. • CPR/AED/First Aid certification. • Proficiency in computer programs. • Strong diplomatic skills (ability to listen, empathize, and respond to participants’ concerns). • Must possess strong communication, interpersonal, attention to detail, and organizational skills. • Bilingual (English/Spanish) is required. Must be able to pass a drug test and background screening. You may visit The Florida Care Provider Background Screening Clearinghouse for more information. https://info.flclearinghouse.com. We are a Drug-Free Workplace, , and we are committed to providing equal employment opportunity for all persons regardless of age, disability, national origin, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, veteran or military status, genetic information or any other status protected by applicable federal, state, or local law.

Responsibilities

The Medical Research Coordinator will support and manage clinical research studies, ensuring compliance with all regulatory guidelines, and coordinating daily activities such as patient screening, recruitment, enrollment, and follow-up. Responsibilities also include maintaining accurate study documentation, serving as a liaison, and managing clinical sample processing and data entry.