Project Coordinator (Clinical Operations)
By GroupA At California, United States
Creation and management of contracts with institutions and vendors
Budget management and accruals and Interfaces with the Accounting Departments to create
Document management (eg Sharepoint, teams, etc)
3+ years of experience within an operational role in the biotechnology/pharmaceutical industry (e.g., medical affairs, clinical operations, clinical research, CRO)
Analytical skills: ability to analyze, sort and prioritize data, create data extracts and or reports from systems
Experience with the following tools: Microsoft Office Suite (Excel, Word, PowerPoint, etc.), MS Teams, Zoom, Ariba, Icertis. SAP, Cybergrants. Smartsheet
Research Project Coordinator - Neurology
By Washington University in St Louis At , St. Louis, 63110, Mo $40,100 - $72,700 a year
Perform data analysis and/or data management for investigators using statistical packages including generation of tables and graphs.
Manage, develop, and coordinate all project activities, serving as the primary contact for external partners.
Manage budgetary expenditures in cooperation with financial manager.
Bachelor's degree and two years of experience; or a master's degree.
For policies, detailed benefits, and eligibility, please visit: https://hr.wustl.edu/benefits/
Prepare regular progress reports and final reports for funding agency.

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are seeking a Clinical Research Project Coordinator to join our team and help us advance our mission of providing innovative treatments to improve patient outcomes. As a Clinical Research Project Coordinator, you will be responsible for managing the day-to-day operations of clinical research projects, including data collection, analysis, and reporting. You will also collaborate with other departments to ensure the successful completion of projects. If you are a highly organized and detail-oriented individual with a passion for clinical research, this could be the perfect job for you!

Overview A Clinical Research Project Coordinator is a professional who is responsible for coordinating and managing clinical research projects. They are responsible for ensuring that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies. They are also responsible for ensuring that the research is conducted in a timely and efficient manner. Detailed Job Description A Clinical Research Project Coordinator is responsible for coordinating and managing clinical research projects. They are responsible for ensuring that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies. They are also responsible for ensuring that the research is conducted in a timely and efficient manner. They are responsible for the day-to-day operations of the research project, including the recruitment of participants, the collection of data, the analysis of data, and the reporting of results. They are also responsible for ensuring that the research is conducted in a safe and ethical manner. Job Skills Required
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of clinical research protocols and regulations
• Knowledge of data collection and analysis techniques
• Knowledge of medical terminology
• Ability to manage multiple projects simultaneously
• Ability to work under pressure and meet deadlines
Job Qualifications
• Bachelor’s degree in a related field such as healthcare, science, or research
• Previous experience in clinical research
• Certification in clinical research
Job Knowledge
• Knowledge of clinical research protocols and regulations
• Knowledge of data collection and analysis techniques
• Knowledge of medical terminology
• Knowledge of clinical research software
Job Experience
• Previous experience in clinical research
• Experience in project management
• Experience in data collection and analysis
Job Responsibilities
• Coordinate and manage clinical research projects
• Ensure that the research is conducted in accordance with the protocols and regulations set by the regulatory bodies
• Recruit participants for the research project
• Collect and analyze data
• Report results of the research
• Ensure that the research is conducted in a safe and ethical manner
• Manage multiple projects simultaneously
• Meet deadlines and work under pressure