Register
Recruit Create CV

Clinical Research Coordinator Jobs in Missouri

Clinical Research Coordinator I - Occupational Therapy
By Washington University in St Louis At , St. Louis, 63110 $46,400 - $69,700 a year
Combination of college education and relevant experience equaling four years may substitute for this requirement
Experience working with adults with neurological disabilities.
Working knowledge of computer programs and systems.
Communication, organizational and interpersonal skills.
For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/
Routinely collects clinical data under clinical research protocols.
Clinical Research Coordinator Jobs
By University of Missouri - Kansas City At , Kansas City, 64110, Mo $50,367 - $91,392 a year
Know Your Rights English Version
Know Your Rights Spanish Version
Salary Range: $50,367 - $91,392
Internal applicants can determine their university title by accessing the Talent Profile tile in myHR.
8:00 a.m. – 5:00 p.m.
Some weeknights or weekends necessary to ensure proper enrollment for clinic trials.
Clinical Research Coordinator Jobs
By The IMA Group At St Louis, MO, United States
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
Additional duties and responsibilities may be assigned as needed.
Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
Clinical Research Coordinator - Remote
By City of Hope At California, United States
Bachelor’s Degree. Experience may substitute for minimum education requirements. (i.e. Associate Degree plus two years of experience.)
Basic education, experience and skills required for consideration:
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Fulfills sponsor requirements related to reportable information, including: AE, unanticipated problems, other information required by the sponsor protocol.
Assist the Epic Protocol Content Administrators (PCAs) with questions regarding the protocol procedural requirements, including lab tests, EKG’s or imaging.

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