Clinical Research Assistant

Covenant Metabolic Specialists

Fort Myers, FLFull-timePosted Apr 7, 2026

40K–50K a year

Behavioral Health Market Context

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Benefits

Dental CoveragePaid Time OffHealth Insurance

Job Description

lsewhere. With over 200 years of combined clinical experience, our expert medical team delivers state-of-the-art therapies and lifestyle guidance to improve metabolic health for patients.

Covenant is seeking a Research Assistant for our facility located in Ft Myers, Florida. This position will assist with our clinical operations by taking patient vital signs and other measurements, performing FibroScans, completing EDC entries, and other duties as needed.

Responsibilities
• Use phlebotomy skills to collect lab specimens from patients.
• Collect vital signs, weight, height, body measurements, EKG, etc. according to study requirements and documents appropriately in source document.
• Upload EKGs to Sponsor specific portals, answer queries as needed, and reorder supplies.
• Perform FibroScans on patients.
• Restock patients’ rooms at the end of each week.
• Enter data into EDC and answers queries as assigned.
• Print and file study specific or patient specific documents.
• Print labs daily from DocuSign as assigned and provide reports to the appropriate Clinical Research Coordinator (CRC).
• Assist in the Lab.
• Update or load documents into the Company’s clinical trial management system as needed.
• Update excel sheets as requested by CRCs.
• Request medical records and follow up as needed.
• Clean exam rooms.
• Help CRCs with any other tasks as needed.
• Other duties as assigned.

Education and Experience
• Associate's degree in a related field (such as Medical Assisting, Nursing, Life Sciences, or Healthcare Administration), preferred.
• Relevant certificates (e.g., Certified Medical Assistant, Emergency Medical Technician) or significant coursework in a related field.
• 1-2 years of experience in a clinical setting or in clinical research preferred.
• Experience performing phlebotomy, EKGs, and other diagnostic procedures is desirable.
• Experience with a Clinical Trial Management System (CTMS) is a plus.
• Experience with specific technology, such as a FibroScan machine, is desirable

Other Skills
• Proficient with Electronic Data Capture (EDC) or Electronic Medical Records (EMR) systems.
• Basic office software (e.g., Microsoft Office Suite, especially Excel).
• Excellent verbal and written communication skills to effectively interact with patients, staff, and sponsors.
• Strong organizational and multitasking skills, with the ability to prioritize tasks in a fast-paced environment.
• Bilingual (English/Spanish) preferred.
• Certifications in CPR, Basic Life Support (BLS), or other relevant healthcare certifications
• Ability to meticulously follow study protocols, document patient data accurately, and manage confidential information.
• Demonstrated ability to work collaboratively in a team and support colleagues in achieving team goals.
• Openness to learning new skills and adapting to changing procedures and protocols.
• Understanding of patient privacy laws (HIPAA) and ethical considerations in clinical research.
• Willingness to undergo background checks and necessary training for compliance with healthcare regulations.

Covenant Metabolic Specialists, LLC is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, genetics, disability, age, veteran status, or any other characteristic protected by law.

Pay: $40,000.00 - $50,000.00 per year

Benefits:
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Education:
• Associate (Preferred)

Experience:
• nursing or medical assistant: 1 year (Preferred)

Work Location: In person

Qualifications

  • Relevant certificates (e.g., Certified Medical Assistant, Emergency Medical Technician) or significant coursework in a related field
  • Proficient with Electronic Data Capture (EDC) or Electronic Medical Records (EMR) systems
  • Basic office software (e.g., Microsoft Office Suite, especially Excel)
  • Excellent verbal and written communication skills to effectively interact with patients, staff, and sponsors
  • Strong organizational and multitasking skills, with the ability to prioritize tasks in a fast-paced environment
  • Certifications in CPR, Basic Life Support (BLS), or other relevant healthcare certifications
  • Ability to meticulously follow study protocols, document patient data accurately, and manage confidential information
  • Demonstrated ability to work collaboratively in a team and support colleagues in achieving team goals
  • Openness to learning new skills and adapting to changing procedures and protocols
  • Understanding of patient privacy laws (HIPAA) and ethical considerations in clinical research
  • Willingness to undergo background checks and necessary training for compliance with healthcare regulations

Benefits

  • Pay: $40,000.00 - $50,000.00 per year
  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Responsibilities

  • This position will assist with our clinical operations by taking patient vital signs and other measurements, performing FibroScans, completing EDC entries, and other duties as needed
  • Use phlebotomy skills to collect lab specimens from patients
  • Collect vital signs, weight, height, body measurements, EKG, etc. according to study requirements and documents appropriately in source document
  • Upload EKGs to Sponsor specific portals, answer queries as needed, and reorder supplies
  • Perform FibroScans on patients
  • Restock patients’ rooms at the end of each week
  • Enter data into EDC and answers queries as assigned
  • Print and file study specific or patient specific documents
  • Print labs daily from DocuSign as assigned and provide reports to the appropriate Clinical Research Coordinator (CRC)
  • Assist in the Lab
  • Update or load documents into the Company’s clinical trial management system as needed
  • Update excel sheets as requested by CRCs
  • Request medical records and follow up as needed
  • Clean exam rooms
  • Help CRCs with any other tasks as needed
  • Other duties as assigned


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