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Clinical Research Coordinator Jobs in Colorado

Assistant Clinical Research Coordinator
By National Jewish Health At Denver, CO, United States
Demonstrates compliance with all state, federal and all other regulatory agency requirements.
Work Experience: Clinical research or clinical experience preferred
Voluntary Benefits, like Accident Insurance, Critical Care and Hospital Indemnity
Complies with regulatory bodies to create and maintain study records, and if applicable, dispensation and accountability of investigational product.
Be available to work as scheduled and report to work on time.
Be willing to accept supervision and work well with others.
Program Coordinator, Clinical Research Administration
By UCHealth At , Denver, 80230, Co $22.14 - $28.78 an hour
2 years clinical research administrative experience
Clinical research experience highly desired
Tuition and continuing education reimbursement
Full suite of voluntary benefits such as identity theft protection and pet insurance
Collaborates with multidisciplinary teams to assist with problem identification and resolution, cost containment issues, implementation of new services, and systems/performance measures.
Serves as a resource to staff regarding departmental/area policies, procedures and services.
Clinical Research Coordinator Jobs
By Cleerly, Inc. At , Denver, Co $69,000 - $128,000 a year
Experience with regulatory and data management aspects of clinical research.
Study Management and Research Operations
Solid computer skills – requirement of MS applications including (but not limited to) MS Project, Word, Excel, Power Point.
Job duties, activities and responsibilities are subject to change by our company.
Manages the study publication process.
Manages communication with key stakeholders, vendors, and third party providers.
Clinical Research Coordinator Jobs
By ALLIANZ RESEARCH INSTITUTE, INC At Aurora, CO, United States
Compensation based on education and related work experience
Minimum 1~ 2 years experienceof clinical research coordinator
The main role of study coordinator but not limited to
- recruit patients to research studies
- coordination of clinical research to ensure research activities comply federal guidelines and institutional policy
- reviewing and comprehending research protocols

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