Clinical Research Coordinator

 ensuring compliance, and improving patient outcomes. The team operates in a dynamic and professional environment, striving to contribute meaningfully to the field of dermatology.

Role Description
This is a full-time, on-site position located in Wellington, FL. The Clinical Research Coordinator will oversee the administration of clinical research studies, ensuring compliance with protocols, regulatory requirements, and company standards. Responsibilities include obtaining patient informed consent, maintaining accurate records, coordinating and conducting study visits, data entry, patient outreach and communication and interacting with clinical trial sponsors and monitors. The role also involves managing research protocols, preparing documentation, and collaborating with medical staff to ensure quality results.

Qualifications
Minimum 1 year CRC experience
Experience with Informed Consent processes and adherence to regulatory guidelines
Demonstrated ability in Research data collection
Strong organizational and communication skills
Detail-oriented with the ability to multitask and manage multiple priorities
Bachelor's degree in a healthcare, science, or related field is preferred
Bilangual English/Spanish required
Phlebotomy trained (certification preferred but not required)