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Experienced Clinical Research Coordinator Jobs

Clinical Research Coordinator 1 Jobs
By Baylor Scott & White Health At , Dallas, 75246
Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
Research certification or other certifications per specialty area preferred.
Proven written and oral communication skills.
Exceptional computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
Clinical Research Coordinator Jobs
By Columbia University Medical Center At , New York, 10032 $35 an hour

528309 Medical Center Pediatrics Full Time Opening on: Aug 2 2022 Grade 103 Add to favorites Favorited View favorites Job Type: Officer of Administration Bargaining Unit: ...

Clinical Research Coordinator Jobs
By Banner Health At , Gilbert, 85234
This position will support clinical trials for solid tumor patients
This position is Monday - Friday 8am-5pm, No weekends, no holidays!
Our organization supports a drug-free work environment.
Clinical Research Coordinator Jobs
By University of Washington At , Seattle, 98195 $4,554 - $6,100 a month
Data & Patient Management – 40%
As a UW employee, you will enjoy generous benefits and work/life programs.
Prior experience working with patients and/or the public or healthcare providers in a healthcare setting.
Prior experience with industry-sponsored clinical trials preferred.
Experience with diabetes technologies including pump and CGM preferred.
Seattle - South Lake Union
Clinical Research Coordinator/Research Audiologist
By Duke University At , Durham, 27710
Enters and collects data, and develops data entry or collection SOPs or tools.
Recognizes and reports security of physical and electronic data vulnerabilities.
Uses systems and system reports to manage research participants activities and charge routing.
Required Qualifications at this Level
Screen participants for complex studies (e.g., procedural and interventional studies).
Develops or helps develop SOPs.
Clinical Research Coordinator Jobs
By Columbia University At , New York $63,000 - $65,000 a year
Bachelor's degree or equivalent in education and experience, plus two years of related experience.
Participates in patient education, obtaining informed consent, ordering pre-randomization tests and dispensing and ordering study drug.
Excellent verbal and written communications skills and attention to detail required.
Computer skills (Microsoft Office suite) required. Must be able to work independently and must strictly adhere to deadlines and protocols.
Good Clinical Practices (GCP) and HIPAA certification required.
Job Type: Officer of Administration
Clinical Research Coordinator Ii
By University of Alabama at Birmingham At , Birmingham

Work Arrangement (final schedule to be determined by the department/hiring manager): Remote/Hybrid Eligible

This position will be responsible for research activities and research documentation processes.

Clinical Research Coordinator Ii
By Legacy Health At , Portland, 97210
Proficient in word processing, spreadsheet management and database management.
Bachelor’s degree in a related field or equivalent healthcare experience.
One year of experience in clinical research coordination.
Excellent interpersonal skills, with proven written and verbal competencies.
Specialized knowledge of the research process and federal regulations.
Good analytical and problem-solving skills.
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 Jobs
By University of Chicago At Chicago, IL, United States
Analyzes protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
Clinical Research Coordinator Jobs
By SQRL At Salt Lake City Metropolitan Area, United States
Gain experience and build a network in an expanding area of clinical research, including cutting-edge vaccine trials
1+ years of experience working as a Clinical Research Coordinator
1+ years of experience with Sponsor backed clinical trials (phases I, II, III, or IV)
$25/hr - $29/hr + bonus (Hourly pay = 1.5x overtime potential!)
Surrounded by an entrepreneurial leadership team motivated to make a difference in people's lives
Partnered with one of the largest clinical research companies in the nation!
Clinical Research Coordinator Jobs
By Colgate-Palmolive At Piscataway, NJ, United States
Moderate experience in clinical research, bio-instrumentation and peer-reviewed publications (preferably with Personal Care/Skin Health products).
2-3 years of functional experience (combination of industry and advanced degree acceptable).
Able to multi-task and manage projects independently.
Excellent communication, presentation and writing skills.
Coordinate in-house testing (as needed) and external clinical/case studies.
Monitor the conduct of external clinical/case studies (travel required as needed).
Clinical Research Coordinator Jobs
By OrthoArizona At Gilbert, AZ, United States
Strong organizational skills and attention to detail to manage multiple tasks efficiently.
Collaborate with the supervising physician and research team to develop, implement, and manage clinical research protocols.
Coordinate and conduct study visits, collect and record accurate data, and ensure compliance with study protocols and regulatory requirements.
Participate in the training and education of study team members, as well as study-related educational sessions for participants.
Previous experience as a Clinical Research Coordinator or in a similar research-related role is preferred.
Knowledge of electronic data capture systems and proficiency in MS Office applications.
Clinical Research Coordinator Jobs
By Axle Informatics At Rockville, MD, United States
Supports the creation and management of clinical websites and web-based tools.
Manages conflicts issues that arise in clinical research setting, by utilizing strong communication and collaboration skills.
Educational Benefits for Career Growth
Assist researchers with study testing, observations data entry and other duties associated with study sessions. 5
Assesses ongoing consent through discussions with participants and reinforcement of education
Create mock ups and visualizations to illustrate to web developers how to execute web enhancements or new web requirements.
Clinical Research Coordinator Jobs
By Medix™ At Houston, TX, United States
Coordinates patient care in compliance with protocol requirements
Disburses investigational drug and provide patient teaching regarding administration and other patient educational needs
Screens potential patients for protocol eligibility
Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Responsible for review of consents to ensure proper execution of the informed consent process for study subjects
Oversees the preparation of orders by physicians to assure that protocol compliance is maintained
Clinical Research Coordinator Jobs
By M3 USA At Chattanooga, TN, United States
Extensive clinical trial knowledge through education and/or experience
Assist management with potential new hire selection and shadowing process.
Clinical skills, including the ability to perform phlebotomy
Successful completion of GCP Certification and Advanced CRC preferred
Minimum 1-2 years of clinical research coordinator experience required
Excellent communication and organizational skills
Clinical Research Coordinator Jobs
By Iowa Oncology Research Association At Des Moines Metropolitan Area, United States
Key data for remote data entry or submit completed case report forms per protocol guidelines.
Collate data for submission to meet protocol requirements.
Assist in administrative responsibilities as assigned.
This job has no supervisory responsibilities.
Answer telephone, screen calls, take messages, and provide information to appropriate staff.
Communicate on a regular basis with investigators and office nurses regarding the availability of clinical studies.
Clinical Research Coordinator Ii (Multiple Vacancies)
By Rutgers University At New Brunswick, NJ, United States
Maintain documentation according to protocols, standard operating procedures, and FDA requirements.
This role requires strong organizational and prioritization skills, as the coordinator will be responsible for managing 4 to 5 concurrent trials.
Excellent interpersonal skills are essential for clear and confident patient interactions.
Experience in cardiology and complex clinical trials is a plus.
Physical Demands: Standing, sitting, walking, talking or hearing. No special vision requirements. Lifting (up to 25 pounds).
Carefully collect, compile and document clinical research data according to the study protocol and sponsor guidelines.
Clinical Research Coordinator Jobs
By care.coach At Millbrae, CA, United States
Strong attention to detail & time management skills
Implement and manage clinical research projects with internal and external stakeholders across the country in hospital and community-based settings
Obtain IRB approval and maintain compliance with OHRP and other federal regulatory requirements
3+ years of research coordination experience and independence (can be pre-doctoral)
Experience with older adults and ab/normal age-related decline
Grant writing and clinical trial (RCT) experience

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