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Initiation Clinical Research Associate Ii Jobs in Arkansas

Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Associate Ii (Home-Base)
By Talentify.io At United States
Utilize systems and technology for account management tasks
Remote work-from-home position with flexible schedules
Comprehensive benefits package including medical, dental, vision, and life insurance
Excellent communication skills, both written and oral
Basic knowledge of Microsoft Office Suite and Windows operating system
Strong problem-solving and conflict resolution skills
Clinical Research Coordinator Ii-Msh-Cs03-12118-013
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Associate Ii
By Reflow Medical At United States
SPECIAL SKILLS, ABILITIES, AND REQUIREMENTS
Coordinates and manages the activities of investigative sites to ensure compliance with study protocol requirements
Supports device management, including device accountability, at the site and Sponsor level
Advanced knowledge and experience with GCP/ICH and local regulations
Experience in web-based data collection applications, knowledge of key areas of Compliance
Previous field monitoring experience required, monitoring of device trials in the cardiovascular space preferred
Clinical Research Coordinator Ii-13400-043
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator Ii-Psychiatry - Ism - Ft - Day
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Research Associate I/Research Associate Ii (Remote)
By OCHIN, Inc. At United States
Demonstrated experience in complex project management and working on a project team.
Working knowledge of research and project management software preferred (e.g., REDCap, EndNote, Zotero, Smartsheet, Microsoft Suite, Twilio, etc.).
Detail-oriented and organized approach to project management.
Manages day-to-day operations of research projects and networks under the supervision of Project Director and/or Lead Investigator.
Manages day-to-day operations of complex research projects and networks. Exercises judgement in taking independent action and seeks advice when appropriate.
Working knowledge of medicine, public health, and health services issues relevant to the application of research.

Are you looking for an exciting opportunity to join a dynamic team of Clinical Research Associates and help shape the future of medical research? We are looking for a Clinical Research Associate II to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate II, you will be responsible for the initiation, monitoring, and close-out of clinical trials. You will also be responsible for ensuring compliance with applicable regulations and guidelines. If you are a motivated individual with a passion for clinical research, this may be the perfect opportunity for you!

Overview The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This role requires a high level of knowledge and experience in clinical research and the ability to effectively manage multiple projects. Detailed Job Description The Initiation Clinical Research Associate II is responsible for the initiation and management of clinical research studies. This includes developing and executing study protocols, managing study budgets, and ensuring compliance with applicable regulations and guidelines. The Initiation Clinical Research Associate II is also responsible for coordinating and managing the activities of the study team, including the clinical research staff, investigators, and other stakeholders. Job Skills Required
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Excellent organizational and project management skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to manage multiple projects simultaneously
Job Qualifications
• Bachelor’s degree in a related field
• At least 3 years of experience in clinical research
• Certification in clinical research (e.g. CCRA, CCRP, etc.)
Job Knowledge
• Knowledge of clinical research principles and practices
• Knowledge of applicable regulations and guidelines
• Knowledge of clinical trial design and data management
• Knowledge of Good Clinical Practice (GCP)
Job Experience
• At least 3 years of experience in clinical research
• Experience in managing clinical research studies
• Experience in coordinating and managing the activities of the study team
Job Responsibilities
• Develop and execute study protocols
• Manage study budgets
• Ensure compliance with applicable regulations and guidelines
• Coordinate and manage the activities of the study team
• Monitor study progress and ensure data accuracy
• Prepare and submit study reports
• Provide training and guidance to study team members