Clinical Research Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
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 Research Coordinator Jobs
By University of Washington At , Seattle, 98195, Wa $5,100 - $5,700 a month
Two to three years of experience in public health, medicine, research OR equivalent education/experience
Conduct active recruitment in clinic and when approved: remotely via phone or Zoom
Experience handling, processing, and transporting human biologic specimens.
Maintain confidentiality of medical/research records as well as our Access database for profiling and tracking of specimens
Support the development and revision of Standard Operating Procedures for various studies
Maintain and implement research protocols for ongoing specimen collection
Sr. Clinical Research Associate (Remote)
By Thrive At Seattle, WA, United States
Assist with essential documents collection, review and archiving (TMF management)
Provide project management support for PTX project team, including vendor oversight
Conduct Site Initiation, Routine, and Close-out monitoring site visits, either on-site or remotely, prepare visit correspondence and records including trip reports
Phases I-IV ONCOLOGY Trial experience
Oversee the conduct of assigned study sites, including ensuring compliance with SOPs, federal and local regulations, and ICH and GCP guidelines
Assist in the review and /or development of clinical trial documents such as study plans and training materials
Clinical Research Coordinator Ii
By Seattle Childrens Hospital At , Seattle, 98105, Wa $67,454 - $101,192 a year
Min to Max Hourly Salary
Min to Max Annual Salary
The union pay ranges can be found on the Seattle Children's website here: WSNA - UFCW
Disclaimer for Out of State Applicants
Seattle Children's is proud to be an Equal Opportunity Workplace and Affirmative Action Employer.
Clinical Research Coordinator Jobs
By Children's National Hospital At , Washington, 20010, Dc
Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
Meets all annual job-related training and compliance requirements.
Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
Consistently demonstrates adherence to the standards for the responsible conduct of research.
Uses research funds and resources appropriately.
Maintains confidentiality of data as required.
Care Management Clinical Support Coordinator (Remote)
By Providence Health Plan At , Vancouver, 98661, Wa
Be responsible for performing duties in support of the core functional areas of care management and other integrated medical management programs
Bachelor's Degree in a Health related field of study -OR - a combination of equivalent education / experience
Providence is calling a Care Management Clinical Support Coordinator who will:
Experience working withlean principles, stewardship, programs and partnership development
Experience working in a challenging and dynamic healthcare environment
Required qualifications for this position include:
Clinical Research Coordinator Jobs
By SRG At Springfield, Illinois Metropolitan Area, United States

Job Title: Clinical Research CoordinatorLocation: Springfield, IL Worksite: OnsiteJob Type: Permanent Full-Time We are searching for a permanent full-time Clinical Research Coordinator who has ...

Account Coordinator/Manager, Clinical Research
By Clinitiative Health Research At Dallas, TX, United States
Works on client clinical trial pipeline to secure study award
Persists to locate appropriate contacts for trial updates and outreach
Demonstrates basic understanding of clinical research
Acts on behalf of sites to sponsors to ensure consideration for feasibility and award
Communicates study updates to sites and other staff members
Completes multiple competing tasks in expected timelines
Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Coordinator Jobs
By Medasource At New York, United States
1+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Ensure data quality and integrity throughout the life of the study.
Collaborate with members of the research and care teams across MSK regarding data input.
Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
Clinical Research / Finance Analyst - Remote, Must Reside In California
By Children's Hospital Los Angeles (CHLA) At Los Angeles, CA, United States

NATIONAL LEADERS IN PEDIATRIC CARE

Clinical Research Coordinator Jobs
By SMCI At San Francisco Bay Area, United States
Education: BS/BA degree in a life science, health science, RN, or related field.
2+ years of professional working experience as a Clinical Research Coordinator.
Working knowledge of GCP and FDA Regulations.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.
Clinical Research Coordinator Jobs
By SeattleNTC At Greater Seattle Area, United States
$25-$30 per hour depending on experience
2+ years of Clinical Research experience
Experience administering questionnaires (for example, WASI-II, other IQ assessments, MADRS, CAPS-5)
Experience with clinical research protocols, regulatory compliance, and submission processes
Mental health experience a plus
Seattle and Bellevue clinics (must be able to work at both)
Clinical Research Coordinator Jobs
By CAMRIS At Bethesda, MD, United States
Knowledge of clinical quality management and systems (such as Veeva, Master Control, etc.) is preferred.
Assist in the management of Division contract records. Tasks include the following:
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at
Minimum of five (5) years of experience in clinical research or a related field.
Excellent communication, grammar and writing skills required.
Demonstrated superior knowledge of research protocols and clinical, scientific and/or medical terminology.
Clinical Research Coordinator - Manager
By Medix™ At San Antonio, Texas Metropolitan Area, United States
Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs;
Obtain patient informed consent according to federal regulations, GCPs and IRB requirements;
Schedule and conduct patient visits according to protocol requirements and timelines;
Read, understand and is able to accomplish protocol specified patient visits and procedures;
Maintain accurate and complete written source documentation of patient visits and protocol related activities;
Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor;
Research Analyst-Project Coordinator (Remote)
By Talentify.io At United States
Strong organizational and time management abilities.
Proficiency in project management software.
Knowledge in areas such as early intervention, special education, educational equity, and program evaluation.
Experience in an education organization or agency.
Strong systems thinking and understanding of project management strategies.
Contribute to research, training, and technical assistance activities in the education field.
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 Analyst *Remote*
By Talentify.io At United States
Communicate extensively with various stakeholders to manage research activities including billing compliance, budgeting, subject tracking, data collection, and sponsor invoicing.
Bachelor's Degree in a health-related field or 4 additional years of related experience.
Three years of IRB, regulatory, or research experience (4 years preferred).
Three years of relevant CTMS experience.
This is a remote position that can be based in any Providence state approved location in the US.
Review clinical research protocol documents and replicate the protocol schedule of events in Velos EResearch CTMS.
Coord,Clinical Research Ii - 100% Remote
By Talentify.io At United States
Track and maintain study-related information in the data management system
Ensure adherence to study protocols and regulatory requirements
Bachelor's degree in a scientific or health-related field, or equivalent experience
1-3 years of related experience
Obtain consent of research participants in accordance with IRB approved protocols and regulations, including HIPAA
Schedule and conduct participant study visits, tests, interviews, and telephone follow-up calls
Clinical Research Coordinator Jobs
By Yuma Clinical Trials At Yuma, AZ, United States

CRC

Clinical Research Trainer - Remote ($59000.00 - $91500.00 / Year)
By Talentify.io At United States
Deliver engaging and logical CRA-sponsored training remotely
Excellent planning and prioritization skills aligned with organizational goals
Develop and update CR education tools and course materials
Schedule MSK-wide CR educational courses for staff
High School Diploma and 2-5 years of relevant experience in training, mentorship, or clinical research
Knowledge of training design, medical terminology, and oncology concepts preferred

Are you looking for a rewarding career in clinical research? We are seeking a Remote Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, ensuring compliance with regulatory standards, and providing support to research teams. If you are passionate about making a difference in the medical field, this is the perfect opportunity for you!

Overview A Remote Clinical Research Coordinator is responsible for coordinating and managing clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. Detailed Job Description The Remote Clinical Research Coordinator is responsible for the coordination and management of clinical research activities in a remote setting. This includes working with clinical research teams, sponsors, and other stakeholders to ensure that research protocols are followed and that data is collected, analyzed, and reported accurately. The Remote Clinical Research Coordinator is also responsible for the development and implementation of research protocols, the collection and analysis of data, and the preparation of reports and presentations. The Remote Clinical Research Coordinator must be able to work independently and collaboratively with other team members. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to work independently and collaboratively
• Excellent organizational and communication skills
• Proficiency in data analysis and reporting
• Ability to manage multiple projects simultaneously
• Knowledge of computer systems and software
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Knowledge of Good Clinical Practice (GCP)
• Ability to work in a remote setting
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of computer systems and software
Job Experience
• At least two years of experience in clinical research
• Experience in data analysis and reporting
• Experience in project management
Job Responsibilities
• Develop and implement research protocols
• Collect and analyze data
• Prepare reports and presentations
• Manage multiple projects simultaneously
• Ensure compliance with clinical research protocols and regulations
• Communicate with clinical research teams, sponsors, and other stakeholders
• Work independently and collaboratively with other team members