Clinical Research

• Plan, organize, and implement recruitment programs to meet targeted enrollment goals for study protocols
• Enroll appropriate subjects in clinical research protocols
• Phone screen patients or caregivers in a caring and empathetic manner
• Correctly document patient information in the computer database
• Schedule and reschedule patient screening and prescreening appointments
• Manage incoming calls from patients interested in research studies
• Evaluate potential subject eligibility through screening interviews, medical record reviews, or discussions with site clinic staff
• Maintain knowledge of clinical research studies and inclusion/exclusion criteria
• Record patient contact status and update database information
• Review, call, and update sponsor patient portals as needed
• Perform other assigned duties

Clinical Research Patient Recruiter

• Report to the principal investigator of a clinical research study
• Perform evaluation duties in preparation for projects
• Oversee screening and enrollment of potential clients for health services protocols
• Develop materials communicating projects to potential clients and their families
• Coordinate site visits and appropriate data collection
• Ensure data quality control and compile regulatory reports
• Coordinate protocol implementation and collaborate with IT, pharmacy, nursing, physician groups, and administration
• Facilitate clinical workflows and electronic health record order sets
• Develop and deliver training for clinical staff
• Supervise research personnel and recruit and train data-gathering assistants
• Manage study documents and budgets and ensure project milestones are met
• Monitor laboratory tests and referrals
• Monitor compliance with federal, state, and university regulations
• Maintain eligibility, informed consent, HIPAA, infection control, and safety documentation
• Prepare and maintain regulatory and compliance documents such as IRB applications
• Collect and analyze clinical trial or medical screening data and create client or medical-record databases
• Collaborate with social workers and professional agencies
• Disseminate study information to clients, families, and the general public
• Draft program reports for publication or public dissemination
• Perform other duties as assigned

Clinical Research Associate

• Assist with various tasks for the clinical research department
• Provide clinical and clerical support to clinical Research Coordinators

Research Clinical Assistant

• Serve as the primary point of contact between investigational sites and the sponsor
• Conduct site selection, initiation, routine monitoring, and close-out visits
• Ensure site compliance with ICH-GCP, SOPs, and regulations
• Maintain documentation in CTMS and eTMF systems
• Support and track site staff training and compliance records
• Monitor patient safety and ensure timely AE/SAE/PQC reporting
• Support subject recruitment and retention efforts
• Oversee drug accountability and proper storage, return, or destruction
• Resolve data queries and drive timely, high-quality data entry
• Document site progress and escalate risks or issues to the clinical team
• Assist with site budgets and timely site payments, as applicable
• Collaborate with CTAs, LTMs, CTMs, and other cross-functional partners

Clinical Research Associate II

• Perform site management activities to support the client's Oncology site success and maintain continuous inspection readiness
• Act as the primary contact between the client's clinical trial team and sites
• Perform remote and on-site monitoring/co-monitoring visits, including Site Qualification, Site Initiation, Interim Monitoring, and Close-Out Visits
• Perform oversight activities to assess monitoring quality and train or mentor less experienced CRAs
• Document monitoring activities and submit or approve visit reports
• Manage site essential document collection and TMF reconciliation with site files
• Support local IRB/Ethics Committee submissions and confirm approvals
• Review site KRI metrics, issues, and action items to detect trends and ensure prompt resolution
• Determine root causes and develop or implement site CAPA plans
• Deliver training on protocols, SOPs, GCPs, and regulations
• Support sites and the client's regulatory inspections
• Contribute to site identification, feasibility, qualification, and activation activities
• Lead site engagement initiatives and foster relationships with Oncology sites and networks

Senior Clinical Research Associate

• Advance AbbVie’s clinical research pipeline and support innovative medicines and solutions
• Serve as the primary point of contact for investigative sites
• Provide clinical trial context and connect stakeholders with investigative sites
• Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles
• Conduct site evaluation, training, routine monitoring, and site closure activities
• Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
• Customize site engagement strategies and track their progress and impact using CRM tools
• Connect study protocols and scientific principles to day-to-day trial execution
• Evaluate recruitment and retention techniques based on the patient disease journey
• Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge
• Mentor and train less experienced CRAs
• Participate in global or local task forces and initiatives
• Conduct continuous risk assessment with the Central Monitoring team
• Resolve site risk signals and implement preventative and corrective action plans
• Identify and evaluate potential investigators and clinical sites
• Ensure data quality, timely data submission, and safety-event reporting and follow-up
• Maintain audit and regulatory inspection readiness
• Manage investigator payments according to executed contract obligations

• Perform research studies under the medical supervision of the Principal Investigator and research director
• Ensure overall successful implementation and ongoing site management of research studies
• Provide coverage in clinics when research staff are out of the office
• Precept new research staff in clinics
• Assist with research projects assigned by the Senior Clinical Research Coordinator III
• Travel to investigators meetings and clinics as required

Clinical Research Coordinator III, RN Required

• Assist with various tasks for the clinical research department
• Provide clinical and clerical support to clinical Research Coordinators
• Travel between clinics

Clinical Research Assistant

• Coordinate patient care by collaborating with medical staff and document according to standards and regulatory guidelines under direction of a mentor or supervisor
• Act as liaison between investigators, Moffitt regulatory staff, and sponsors
• Assist to screen, enroll, and follow study subjects while ensuring protocol compliance and close monitoring
• Manage data and source documentation and adverse experience reporting
• Perform administrative duties requiring analysis, sound judgment, and knowledge of study protocol
• Implement and coordinate research, including administrative procedures, under general supervision and direction from the supervisor and Principal Investigator

Clinical Research Coordinator I – Myeloma/Lymphoma

• Advance AbbVie's clinical research pipeline and support innovative medicines and solutions
• Serve as the primary point of contact for investigative sites
• Provide contextual information on clinical trials and connect stakeholders with investigative sites
• Align, train, and motivate site staff and principal investigators on trial goals, protocols, and patient treatment principles
• Conduct site evaluation, site training, routine monitoring, and site closure monitoring
• Ensure compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
• Develop and customize site engagement strategies
• Gather local and site insights and use CRM tools to track progress and measure impact
• Connect study protocols and scientific principles to day-to-day trial execution
• Evaluate recruitment and retention techniques based on the patient disease journey
• Develop therapeutic-area, asset, clinical-landscape, and patient-journey knowledge
• Mentor and train less experienced CRAs and contribute to their development
• Participate in global/local task forces and initiatives as assigned
• Conduct continuous risk assessment with the Central Monitoring team
• Resolve site risk signals and implement preventative and corrective action plans
• Identify, evaluate, and recommend potential investigators and sites
• Ensure quality and timely submission of site data and safety-event reporting
• Maintain audit and regulatory inspection readiness
• Manage investigator payments according to executed contract obligations, as applicable

Clinical Research jobs in Florida

Clinical Research Patient Recruiter

Clinical Research Associate

Research Clinical Assistant

Clinical Research Associate II

Senior Clinical Research Associate

Clinical Research Associate II

Clinical Research Coordinator III, RN Required

Clinical Research Assistant

Clinical Research Coordinator I – Myeloma/Lymphoma

Clinical Research Associate II – Neurology