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Clinical Research Trials Coordinator Jobs

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.

Project Associate (Remote), Clinical Trials Office
By The Rector & Visitors of the University of Virginia At , $65,000 - $75,000 a year
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Knowledge of GCPs governing clinical research.
Senior Project Manager, Rwe Clinical Trials, Remote
By WALGREENS At , Deerfield, 60015 $143,460 - $196,010 a year
Bachelor’s degree in Life Sciences or related field and at least 4 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (ie. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
May manage a team as and when required
Identify changes in scope and manage the change control process, as necessary
Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Covington, LA, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Research Data Assistant - Clinical Trials (Full Time, Day Shift)
By Nicklaus Children's Hospital At , Miami, 33155
High School education or equivalent
Assists study staff with any concerns or questions by promptly providing the information and feedback as requested
Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.
Provides auditable trail of documentation with consistency among data base, records and required reports
Provides reports on grant progress and assists in troubleshooting
Serves as liaison for Research Institute with all departments involved with the study.
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 I
By Seattle Childrens Hospital At , Seattle, 98105, Wa $55,765 - $83,637 a year
Bachelor's Degree in related discipline, or equivalent combination of education and experience.
Prior experience in research or a related field/setting.
Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments.
Min to Max Hourly Salary$26. 81 - $40.21 /hr
Min to Max Annual Salary$55,764.80 - $83,636.80 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Clinical Trials Research Nurse
By Premier Health At , Centerville, 45459, Oh
Current CPR certification required at the time of hire.
1 - 3 years of job-related experience
Effective interpersonal and communication skills
Must be able to multitask with constant interruptions while maintaining a pleasant demeanor.
CLINICAL TRIALS RESEARCH NURSE / RN
Full Time 8am-4:30pm / 80 Hours per Pay
Clinical Research Coordinator Assistant
By University of California - Irvine At , Irvine, Ca $26.60 - $43.82 an hour
Background Check and Live Scan
Legal Right to work in the United States
California Child Abuse and Neglect Reporting Act
$26.60 - $43.82 (Hourly Rate)
Assistant Clinical Research Coordinator
By Stanford University At Stanford, CA, United States
Advanced computer skills and demonstrated experience with office software and email applications
General knowledge of medical terminology.
Excellent organizational skills and attention to detail
Strong verbal and written communication skills
Excellent customer service and interpersonal skills
May require extended or unusual work hours based on research requirements and business needs.
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.
Project Manager, Rwe Clinical Trials (Remote)
By Walgreens At Deerfield, IL, United States
Bachelor’s degree in Life Sciences or related field and at least 2 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (i.e. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
Identify changes in scope and manage the change control process, as necessary
Experience collaborating with others to deliver results to meet timeline, metrics and budget.

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team