Register
Recruit Create CV

Clinical Research Coordinator Jobs

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 Coordinator I/Ii
By Fred Hutch At Seattle, WA, United States
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.
Minimum two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
Knowledge of clinical trials records, procedures, and computerized data processing systems. Demonstrated knowledge of how to synthesize study conduct.
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.
Part Time Clinical Research Coordinator
By Medasource At United States
3+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Must be available during business hours
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.
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;
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 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-Iii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3-5 years clinical 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
Bachelor’s degree plus 5 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management and data collection
Knowledge and skill with word processing, spreadsheet, database, and e-mail computer software (e.g., Microsoft Word, Excel, Access, Outlook)
UAMS offers amazing benefits and perks
Clinical Research Coordinator Jobs
By Yuma Clinical Trials At Yuma, AZ, United States

CRC

Junior Clinical Research Coordinator
By Axiom Resource Management At , Nellis Afb, 89191
Coordinate with study auditors, regulatory agencies, collaborators, and sponsors in management of research studies.
Must have current Basic Life Support (BLS) certification within 15 days of hire.
Superb organization skills with a high level of attention to detail.
Refined interpersonal and communication skills.
Experience working within the Military Healthcare System preferred.
Send resume and salary requirements to:
Clinical Research Coordinator 046705 Jobs
By Wayne State University At , Detroit From $51,373 a year

H06 - School of Medicine

Hospital, outpatient clinic and office environments.

Clinical Research Coordinator Jobs
By Sundance Clinical Research At Greater St. Louis, United States

Experienced Clinical Research Coordinator (CRC)

Associate Clinical Research Coordinator
By Rush University Medical Center At , Chicago, 60612

Job Title: Associate Clinical Research Coordinator Department: Psychiatry Admin Shift: 1st Specialty: Research Job Number: 2023-2846 Date Posted: 08/08/2023 Position Type: Research Job ...

Clinical Research Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

Clinical/Translational Research Coordinator I - Asthma Research
By Vanderbilt University Medical Center At Nashville, TN, United States
Procures equipment and supplies needed to fulfill project requirements
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Specific Tasks and Skills Include But Are Not Limited To:
Communication (Fundamental Awareness): Clearly, effectively and respectfully communicates to employees or customers.
Discover Vanderbilt University Medical Center:

Are you looking for an exciting opportunity to make a difference in the medical field? We are seeking a Clinical Research Coordinator to join our team and help us advance medical research. You will be responsible for managing clinical trials, coordinating patient visits, and ensuring compliance with regulatory standards. If you have a passion for helping others and a commitment to excellence, this could be the perfect job for you!

A Clinical Research Coordinator (CRC) is responsible for the coordination and management of clinical trials and research studies. They are responsible for ensuring that the research is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practice (GCP).

What is Clinical Research Coordinator Skills Required?

• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of medical terminology
• Knowledge of clinical research regulations and guidelines
• Proficiency in computer applications
• Ability to manage multiple tasks and prioritize
• Ability to work in a fast-paced environment

What is Clinical Research Coordinator Qualifications?

• Bachelor’s degree in a health-related field
• Certification in clinical research (CCRC)
• Previous experience in clinical research

What is Clinical Research Coordinator Knowledge?

• Knowledge of clinical research protocols
• Knowledge of clinical trial design and data management
• Knowledge of medical terminology
• Knowledge of Good Clinical Practice (GCP)

What is Clinical Research Coordinator Experience?

• Previous experience in clinical research
• Previous experience in data management
• Previous experience in clinical trial design

What is Clinical Research Coordinator Responsibilities?

• Develop and implement clinical research protocols
• Monitor clinical trial progress and data
• Ensure compliance with applicable regulations and GCP
• Prepare and submit regulatory