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Clinical Research Jobs in Florida

Clinical Research Nurse Jobs
By Atrium Health At , Charlotte, 28204
Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
Coordinates with Investigational Pharmacy for subjects to receive required drugs.
Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.
Clinical Research Regulatory Manager
By MBO Partners At Charlotte, NC, United States
5-10 years of clinical trial regulatory management experience.
Quality Management System/Regulatory Compliance Program
5 Years minimum regulatory experience in clinical trials
Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Experience gained from multiple perspectives: industry sponsor, CRO, academic, government or site level
Has GCP training and follows GCP guidelines and other guidelines related to the conduct of human subject’s research
Clinical Research Assistant, Baptist Health Research Institute, Full-Time, Days, Downtown Jacksonville
By Baptist Health At Jacksonville, FL, United States
Participates in conducting literature reviews, collect, and analyze all data related to study including patient recruitment and finance.
Manages and responds to project related e-mails, attend project meetings develop minutes, monitor the project budget.
Experience in a clinical setting
Contacts patient follow-up phone calls.
Compiles data for progress reports.
Performs miscellaneous job-related duties as assigned
Clinical Research Nurse Jobs
By Atrium Health At , Charlotte, 28203, Nc
Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
Coordinates with Investigational Pharmacy for subjects to receive required drugs.
Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.
Clinical Research Coordinator Ii - Institute For Clinical & Translational Research
By Johns Hopkins All Children's Hospital At , Saint Petersburg, 33701, Fl
Demonstrates knowledge and skills in accordance with Good Clinical Practice (GCP) guidelines, HIPAA, FDA regulations and other federally mandated guidelines
3 years of prior clinical research coordination or nursing experience required
Proficient knowledge of medical terminology and human subject research
Bachelor’s degree in science or health related field
Must be comfortable working with patient populations
Ability to follow protocols and directions very closely
Associate Clinical Research Coordinator-Cerebrovascular Diseases Research
By Mayo Clinic At , Jacksonville, 32224, Fl $22.91 - $33.27 an hour

Bilingual Spanish/English required for this position.

Affirmative Action and Equal Opportunity Employer

Are you looking for a career that combines your passion for science with the opportunity to make a real difference in people's lives? Join our team as a Clinical Research Associate and help us develop treatments that will improve the lives of patients around the world!

Overview of Clinical Research Clinical research is a field of healthcare science that focuses on the evaluation of new medical treatments, drugs, and devices. Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. Detailed Job Description of Clinical Research Clinical research professionals are responsible for designing and conducting clinical trials, collecting and analyzing data, and reporting results. They must ensure that all research is conducted in accordance with ethical and legal standards. Clinical research professionals must also be able to communicate effectively with other healthcare professionals, patients, and sponsors. Clinical Research Job Skills Required
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Ability to analyze and interpret data
• Ability to communicate effectively
• Ability to work independently
• Attention to detail
• Problem-solving skills
• Computer skills
Clinical Research Job Qualifications
• Bachelor’s degree in a related field
• Master’s degree in a related field
• Certification in clinical research
• Experience in clinical research
Clinical Research Job Knowledge
• Knowledge of medical terminology
• Knowledge of clinical trial design and methodology
• Knowledge of clinical research regulations
• Knowledge of data analysis techniques
Clinical Research Job Experience
• Experience in clinical research
• Experience in data analysis
• Experience in project management
• Experience in report writing
Clinical Research Job Responsibilities
• Design and conduct clinical trials
• Collect and analyze data
• Report results
• Ensure compliance with ethical and legal standards
• Communicate effectively with other healthcare professionals, patients, and sponsors
• Monitor patient safety during clinical trials
• Prepare and submit reports to regulatory agencies