Clinical Research Coordinator/Project Manager
By K2 Medical Research At Orlando, FL, United States
Strong time management and organizational skills In depth knowledge of industry regulations
Outstanding verbal and written communication skills
Excellent interpersonal and customer services skills
Prior experience in a clinical environment preferred. Experience in clinical research is ideal.
LPN, RN, or other medical licensure or certification preferred.
Strong working knowledge of GCP and FDA guidelines
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.
Coordinator - Research Jobs
By Atrium Health At , Charlotte, 28204
Assists in providing patient education and benefits and risks of participating in a clinical drug trial.
Determines protocol-related needs to conduct the trial and orders supplies and equipment.
Recruits and screens potential patients and obtains informed consent.
Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.
Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.
Schedules patient visits and laboratory and diagnostic test procedures.
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 Crc - Remote | Wfh
By Get It Recruit - Healthcare At Pompano Beach, FL, United States

Are you passionate about making a difference in the field of healthcare? Do you thrive on engaging with patients and ensuring top-notch research protocols? We have an exciting opening for a Clinical ...

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.
Clinical Coordinator Jobs
By Women's Care At St Petersburg, FL, United States
Ability to use a computer and enter data in a medical management application
Manages clinical staff at each assigned location and is available for any clinical related issues that arise during patient care.
Prioritizes patient safety including creating a safe clinical environment for patients in accordance with industry standards, certifications, and WCF policies.
AIUM recertification – complete application for recertification with help from lead sonographer every 3 years
LPN with experience may substitute for RN
Minimum of one year nursing experience in a clinic environment
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
Remote Part-Time Clinical Research Coordinator Ii
By Envision Healthcare At Fort Lauderdale, FL, United States
Highly attentive to detail with strong problem-solving abilities and demonstrated organizational skills.
Bachelor’s Degree in Healthcare or Science and 4+ years' related experience; or an equivalent combination of education and experience as described.
Review and be familiar with all prospective protocol patients’ charts to evaluate protocol eligibility, order necessary tests per protocol requirements.
Supervise daily operations of CRC at their site and report entity activity to the Project Manager daily.
Oversee CTMS (Study Manager) to make sure data is entered within 48 hours of patient visits.
Obtain follow-up information on subject(s) according to protocol requirements.
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

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
Research Coordinator Jobs
By Hospital for Special Surgery At , West Palm Beach, Fl
Oversees and conducts the informed consent process on studies as appropriate (requires appropriate training and certification of human research subjects training).
Spearheads efforts to meet patient enrollment targets related to independent research studies. To that end, develops and implements various recruitment strategies.
Ensures accuracy of personnel transcribing data from paper case report form (CRF) into an electronic format.
Conducts study specific team meetings to ensure timely progress of patient enrollment and study activities.
Assist Principal Investigator with writing/editing abstracts and manuscripts as needed.
Assists in patient care coordination by assuring patients complete patient reported outcomes prior to office visits.
Clinical Research Specialist Jobs
By croxconsulting At Naples, FL, United States
Knowledge and Skill Requirements/Specialized Courses and/or Training:
·Manage Investigator-Initiated clinical research studies.
·Lead required cross-functional research meetings to discuss studies and get input from product managers.
·Manage data collection compliance via tracked milestones.
·Responsible for the execution of clinical projects while adhering to budget, scope and schedule requirements.
•4 years of relevant clinical research experience required

Are you looking for an exciting opportunity to make a difference in the lives of patients? We are seeking a Clinical Coordinator to join our research team and help us develop innovative treatments for a variety of medical conditions. As a Clinical Coordinator, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements, and providing support to research staff. If you are passionate about making a difference in the lives of patients, this is the perfect job for you!

Overview Research Clinical Coordinators are responsible for coordinating and managing clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. Detailed Job Description Research Clinical Coordinators are responsible for the planning, implementation, and management of clinical research projects. They are responsible for ensuring that all research protocols are followed, that data is collected and analyzed correctly, and that the research is conducted in a safe and ethical manner. They may also be responsible for recruiting and training research staff, managing budgets, and ensuring that all regulatory requirements are met. They must also ensure that all research results are accurately reported and that all research activities are conducted in compliance with applicable laws and regulations. Job Skills Required
• Excellent organizational and communication skills
• Ability to manage multiple projects and tasks simultaneously
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Ability to work independently and as part of a team
• Ability to work with a variety of stakeholders
• Ability to analyze and interpret data
• Knowledge of budgeting and financial management
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research or related field (preferred)
Job Knowledge
• Knowledge of clinical research protocols and procedures
• Knowledge of applicable laws and regulations
• Knowledge of budgeting and financial management
• Knowledge of data analysis and interpretation
Job Experience
• At least two years of experience in clinical research
• Experience in recruiting and training research staff
• Experience in managing research budgets
• Experience in ensuring regulatory compliance
Job Responsibilities
• Plan, implement, and manage clinical research projects
• Ensure that all research protocols are followed
• Collect and analyze data accurately
• Ensure that research is conducted in a safe and ethical manner
• Recruit and train research staff
• Manage research budgets
• Ensure that all regulatory requirements are met
• Report research results accurately
• Ensure that all research activities are conducted in compliance with applicable laws and regulations