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 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