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Experienced Clinical Research Coordinator Jobs in Florida

Clinical Research Coordinator Jobs
By Nemours At , Orlando, 32827, Fl
Previous research experience, including qualitative interviewing strongly preferred
Minimum of a bachelor's degree in psychology, pre-med, public health, or related.
Must be able to effectively use Microsoft computer software, SPSS, and REDCap.
Must be able to coordinate and establish priorities among diverse tasks.
Clinical Research Coordinator 2 Jobs
By University of Miami At Miami, FL, United States
Any appropriate combination of relevant education, experience and/or certifications may be considered.
Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
Assist principal investigators, project managers in coordinating Federal and/or industry-sponsored research studies.
Maintains study binders and filings according to protocol requirements, UM and department policy.
Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
Minimum 2 years of relevant experience.
Clinical Research Coordinator - 207479
By Medix™ At Lauderdale Lakes, FL, United States
• Have clinical research experience
• Hoping to gain new clinical trial experience
Ability to work independently and as part of a team.
Part time, working 2 days a week 8a-5p (~16 hours per week)
• Located in Fort Lauderdale
• Looking to work 2 weekdays per week
Clinical Research Coordinator Jobs
By Integrated Oncology Network At Lake City, FL, United States
Overseeing the smooth running of clinical trials
Collecting, coding, and analyzing data obtained from research
Informing participants about study objectives
Monitoring research participants to ensure adherence to study rules
Adhering to research regulatory standards
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation
Clinical Research Coordinator Jobs
By OnesourcePCS, LLC At Patrick AFB, FL, United States
Assist with the administrative management of active research protocols as well as contribute to the administration of developing research protocols.
Competitive Compensation& Exceptional Comprehensive Benefits!
Annual CME Stipend and License/Certification Reimbursement!
General medical ethics, telephone etiquette and excellent communication and customer services skills.
At least 3 years of experience within the last 4 years. Prior experience within the DoD/VA systems of care stronglypreferred.
Paid Vacation, Paid Sick Time and 11 Paid Federal Holidays!
Clinical Research Coordinator Jobs
By Jobot At Aventura, FL, United States
Coordinate and manage all aspects of clinical research studies, including patient screening, enrollment, and follow-up
Ensure compliance with HIPAA guidelines and other regulatory requirements
2+ years of experience in clinical research coordination, with a focus on dermatology research (Clinical Research is a must)
Strong knowledge of clinical study research processes and procedures
Excellent organizational and communication skills
Familiarity with HIPAA guidelines and other regulatory requirements
Clinical Research Coordinator Jobs
By Bay Area Arthritis and Osteoporosis At Brandon, FL, United States

BAAO will negotiate salary according to candidate's experience

BAAO is only open 4 days a week (Mon-Thur) giving a 3-day weekend to balance family life

Clinical Research Coordinator Jobs
By CRO Strategies At Miami, FL, United States
Overseeing the smooth running of clinical trials.
Collecting, coding, and analyzing data obtained from research.
Informing participants about study objectives.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
Ops Clinical Research Coordinator
By University of Florida At , , Fl $24.90 - $29.69 an hour
Works with the PI/ research manager(s) to develop and implement recruitment strategies in accordance with IRB requirements and approvals.
Works with the PI/lead coordinator(s) to manage the day-to-day activities of the study including problem solving, communication and protocol management.
Clinical-trials management systems and survey tools such as Qualtrics
Assists the PI and research managers(s) in reviewing protocols
Collaborates with the research manager(s) to prepare a categorized budget and justification.
Collaborates with the PI and research manager(s) to prepare IRB and any other regulatory submission documents as required by the protocol.
Clinical Research Coordinator Jobs
By Intellectt Inc At Charlotte, NC, United States

Title: Clinical Research Coordinator Duration: 2 Years Location: Charlotte, NC Job Summary The Clinical Research Coordinator will be an essential team member in active clinical research, ...

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
Clinical Research Coordinator Jobs
By Ascendo Resources At Miami-Fort Lauderdale Area, United States
Knowledge of GCP guidelines and regulatory requirements for clinical research studies
Ensure compliance with regulatory requirements
4+ years experience in coordinating clinical research studies
Communication, organizational, and problem-solving skills
Coordinate and oversee clinical research studies in dermatology
Recruit and screen study participants

Are you an experienced Clinical Research Coordinator looking for a new challenge? We are looking for a motivated individual to join our team and help us conduct clinical research studies. You will be responsible for coordinating all aspects of the clinical research process, from protocol development to data collection and analysis. If you have a passion for clinical research and are looking for an exciting opportunity, this is the job for you!

Overview Experienced Clinical Research Coordinators are responsible for managing and coordinating clinical research projects. They are responsible for ensuring that all research activities are conducted in accordance with applicable regulations and guidelines. They must be knowledgeable in clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP). Detailed Job Description Experienced Clinical Research Coordinators are responsible for the planning, implementation, and management of clinical research projects. They must ensure that all research activities are conducted in accordance with applicable regulations and guidelines. They must be knowledgeable in clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP). They must be able to effectively communicate with research staff, sponsors, and other stakeholders. They must be able to develop and maintain effective working relationships with research staff, sponsors, and other stakeholders. Job Skills Required
• Knowledge of clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Excellent communication and interpersonal skills
• Ability to develop and maintain effective working relationships with research staff, sponsors, and other stakeholders
• Ability to manage multiple projects simultaneously
• Ability to work independently and as part of a team
• Strong organizational and problem-solving skills
• Proficiency in Microsoft Office Suite
Job Qualifications
• Bachelor’s degree in a related field
• At least 3 years of experience in clinical research
• Certification in Clinical Research Coordination (CCRC) or Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical research protocols, regulatory requirements, and Good Clinical Practice (GCP)
• Knowledge of clinical trial design, data management, and statistical analysis
• Knowledge of medical terminology and clinical terminology
• Knowledge of medical ethics and patient privacy regulations
Job Experience
• At least 3 years of experience in clinical research
• Experience in clinical trial design, data management, and statistical analysis
• Experience in developing and managing clinical research projects
• Experience in working with sponsors and other stakeholders
Job Responsibilities
• Develop and manage clinical research projects
• Ensure that all research activities are conducted in accordance with applicable regulations and guidelines
• Develop and maintain effective working relationships with research staff, sponsors, and other stakeholders
• Monitor and report on the progress of clinical research projects
• Prepare and submit reports to sponsors and other stakeholders
• Ensure compliance with applicable regulations and guidelines
• Provide guidance and support to research staff
• Maintain accurate and up-to-date records