Coord,Clinical Research Ii - 100% Remote
By Talentify.io At United States
Track and maintain study-related information in the data management system
Ensure adherence to study protocols and regulatory requirements
Bachelor's degree in a scientific or health-related field, or equivalent experience
1-3 years of related experience
Obtain consent of research participants in accordance with IRB approved protocols and regulations, including HIPAA
Schedule and conduct participant study visits, tests, interviews, and telephone follow-up calls
Clinical/Translational Research Coord I
By Vanderbilt University Medical Center At Nashville, TN, United States
Communicates a basic knowledge and understanding of the management and implementation of clinical/translational research operations
Procures equipment and supplies needed to fulfill project requirements
Participates in the determination of eligible candidates for study participation, assuring participants fulfill eligibility requirements
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance
Participates in and maintains certifications, licensure and credentialing as required by Vanderbilt, the department and Sponsor
Furthers knowledge base by attending a Basic Research 101 within first three months of employment date
Clinical Program Coord Jobs
By One Call At Jacksonville, FL, United States
Excellent time management skills with a proven ability to meet deadlines.
General Knowledge, Skills & Abilities
Associate’s degree is required; Bachelor’s degree is preferable; or the equivalent combination of education, training, and work experience.
Opportunities to work from home
Tuition Reimbursement Program including certifications
Communicates Gold Standard Review™ results to Adjuster and/or Case Manager, including any outstanding provider or reviewer requests for information.
Research Intermediate Supr 233597 Jobs
By Michigan Medicine At Ann Arbor, MI, United States
Supervisory and project management experience
One or more years staff management experience
Develop, manage, and maintain imaging databases and associated protocols for storing MRI and PET imaging.
Confident and initiative-taking with excellent multi-tasking ability and record-keeping skills.
Outstanding organizational skills with meticulous attention to detail.
Professional demeanor and excellent interpersonal and communication skills
Research & Admin Coord In One Welfare & Sustainability
By The Ohio State University At , Columbus, 43210, Oh $32,025 - $42,675 a year
The targeted hiring range for this position is $32,025 - $42,675 annually, commensurate with education and experience
Excellent oral and written communication skills, ability to work cooperatively with faculty, staff, and external stakeholders
Experience managing administrative tasks associated with research and outreach
excellent oral and written communication skills, ability to work cooperatively with faculty, staff, and external stakeholders
experience managing administrative tasks associated with research and outreach
Advanced training (e.g. MS or a PhD) in a field relevant to the welfare of animals

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Coordinator Intermediate to join our team and help us advance our research initiatives. You will be responsible for coordinating and managing clinical research projects, ensuring compliance with applicable regulations, and providing support to research staff. If you have a passion for clinical research and are looking for a challenging and rewarding career, this could be the perfect job for you!

Overview Clinical Research Coord Intermediate 226121 is responsible for coordinating and managing clinical research studies, including the collection and analysis of data, and the preparation of reports. This position requires a high level of knowledge and experience in clinical research, as well as excellent organizational and communication skills. Detailed Job Description Clinical Research Coord Intermediate 226121 is responsible for the coordination and management of clinical research studies. This includes the collection and analysis of data, the preparation of reports, and the maintenance of records. The position requires a high level of knowledge and experience in clinical research, as well as excellent organizational and communication skills. The Clinical Research Coord Intermediate 226121 is also responsible for ensuring that all research protocols are followed, and that all data is collected and analyzed in accordance with applicable regulations and guidelines. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Excellent organizational and communication skills
• Ability to analyze and interpret data
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Knowledge of computer software programs, such as Microsoft Office
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (preferred)
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of computer software programs, such as Microsoft Office
• Knowledge of medical terminology
Job Experience
• At least two years of experience in clinical research
Job Responsibilities
• Coordinate and manage clinical research studies
• Collect and analyze data
• Prepare reports
• Maintain records
• Ensure that all research protocols are followed
• Ensure that all data is collected and analyzed in accordance with applicable regulations and guidelines