Clinical Research Coordinator Jobs
By Advarra At Indianapolis, IN, United States
Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
Performs duties and responsibilities in a highly organized manner.
Maintain up-to-date working knowledge of regulatory compliance guidelines as defined by the federal regulations, IRBs, and state laws.
3 years of gene therapy or CNS experience required.
CCRP/CCRC/SOCRA certifications or equivalent preferred
Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Clinical Research Coordinator Jobs
By AION Biosystems At Albany, New York Metropolitan Area, United States
●Proficient in Microsoft Office including Word, Excel, Project and PowerPoint, Data management platforms, EMR systems
A combination of education and experience may be considered
●Ensure remote patient monitoring platforms are integrated between the hospital system and Idion
●Maintain completeness of site documents and manage patient and study data
●Ability to prioritize assignments, manage time efficiently and assist in project oversight to meet established deadlines
●Attention to detail with outstanding organizational skills
Clinical Research Coordinator Jobs
By University of Louisville At Center, IN, United States
Maintain in-depth knowledge of protocol requirements and complete all required training prior to performing tasks.
Collect, document, and analyze data obtained from research studies.
Screen patients for entry into clinical studies and assess patients at each visit regarding compliance with protocol, complications, and difficulties.
Clinical Research Coordinator I
By The Geneva Foundation At , Fort Bragg, 28310, Nc $43,800 - $53,800 a year
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Knowledge of CFR, GCP and ICH guidelines
Promote safety and confidentiality of research participants at all times
Clinical Research Coordinator Jobs
By Indiana University At , Indianapolis, 46202, In
Combinations of related education and experience may be considered
For full-time staff employees, Indiana University offers a wide array of benefits including:
Stays up to date with knowledge of regulatory affairs and/or issues.
Bachelor's degree in science or a health-related field and 2 years of clinical research experience OR
Associate degree in science or a health-related field and 3 years of clinical research experience
SOCRA/ARCP Clinical Research Certification upon date of hire

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