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Clinical Research Trials Coordinator Jobs in Nebraska

Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Grand Island, NE, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Senior Clinical Research Coordinator
By Velocity Clinical Research, Inc. At Omaha, NE, United States
Mentor and train staff in the conduct of clinical trials, protocol requirements, communication, and trial management skills
Apply project management concepts to manage risk and improve quality in the conduct of a clinical research study
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Develop, coordinate, and implement research and administrative strategies to successfully manage assigned protocols.
Advanced knowledge of medical terminology
Advanced verbal, written, and organizational skills
Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Omaha, NE, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Clinical Research Coordinator Jobs
By Apsida Life Science At Nebraska, United States
At least 1 year experience as a Clinical Research Coordinator
Demonstrated computer proficiency, specifically with Microsoft Office
I look forward to hearing from you!

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