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 join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team