Clinical Research Assistant

*** Please, ONLY apply if you are CURRENTLY living in SouthWest, Florida (Naples preferred).***

No relocation assistance! No sponsoring!

No remote work! Must come onsite 40 hours per week!

***DO NOT APPLY IF YOU LIVE OUTSIDE OF NAPLES!****

Overview

Essence MD Research is seeking a dedicated and detail-oriented Clinical Research Assistant to join our small, yet dynamic team. In this role, you will be responsible for overseeing Pulmonary clinical trials and ensuring compliance with regulatory requirements. You will work closely with the Principal Investigator, Site Director, and the Clinical Research Staff to facilitate clinical trial operations.

Duties

• Coordinate and manage all aspects of clinical trials, including study design, implementation, and monitoring.
• Ensure compliance with HIPAA regulations and maintain confidentiality of patient information.
• Supervise research staff and provide training on protocols and procedures.
• Conduct blood sampling and perform phlebotomy as required for study participants.
• Monitor patients throughout the trial, recording vital signs and any adverse reactions.
• Manage compliance with regulatory guidelines and institutional policies related to clinical research.
• Collaborate with investigators to prepare study documentation, including informed consent forms and case report forms.
• Maintain accurate records of study data, ensuring all information is complete and up-to-date.
• Assist in the recruitment and screening of study participants.

Qualifications

• Experience in clinical trials or clinical development is preferred.
• Familiarity with clinical laboratory procedures and compliance management.
• Strong understanding of HIPAA regulations regarding patient confidentiality.
• Excellent organizational skills with attention to detail.
• Ability to foster a collaborative work environment.
• Strong communication skills, both verbal and written, to interact effectively with patients and team members.
• Administrative background is a plus.
• Regulatory Affairs experience is a plus.
• Monday through Friday only! 9-5pm.

If you are passionate about advancing medical research through effective coordination of clinical trials, we encourage you to apply for this rewarding opportunity.

Job Type: Full-time

Pay: From $20.00 per hour

Expected hours: 40 per week

Benefits:

• Paid time off

Work Location: In person