Senior Clinical Research Coordinator - Trial Operations Lead

Care Access; Tampa (FL); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

PTO & Holidays

Employer paid medical, dental, vision

HSA/FSA options

Disability insurance

401(k) with company match

Job summary

Care Access is hiring a Clinical Research Coordinator to screen, enroll, and monitor study subjects in compliance with GCP and regulatory standards. The role is on-site with limited travel and involves collaboration with investigators and study staff.

You will support data entry, regulatoryDocs, recruitment, and site operations, ensuring patient safety and protocol adherence in a fast-paced environment at multiple US locations.

Qualifications

• Bachelor’s degree or equivalent combination of education, training and experience.
• Minimum 3 years of Clinical Research Coordinator experience.
• Phlebotomy experience required.
• Recent phlebotomy experience preferred for California/Louisiana/Washington/Nevada roles.

Responsibilities

• Prioritize activities with protocol timelines.
• Maintain FDA and ICH compliance in all trial activities.
• Ensure effective relationships with participants and study staff.
• Balance protocol needs with patient experience and address concerns.
• Interact professionally with patients, representatives, investigators and Care Access Research personnel.
• Coordinate site visits and monitor visits with staff and Sponsor/CRO.

Skills

GCP knowledge

FDA regulations

ICH guidelines

Clinical research coordination

Regulatory documentation

Data entry

Communication

Team leadership

Phlebotomy

Time management

Education

Bachelor’s degree or equivalent

3 years CRC experience

Phlebotomy experience

Care Access CRC experience

Tools

Clinical trials database

IVR systems

Electronic data capture (EDC)

MS Word

Excel

Job description

Care Access is hiring a Clinical Research Coordinator to screen, enroll, and monitor study subjects in compliance with GCP and regulatory standards. The role is on-site with limited travel and involves collaboration with investigators and study staff.

You will support data entry, regulatoryDocs, recruitment, and site operations, ensuring patient safety and protocol adherence in a fast-paced environment at multiple US locations.