[Remote] Remote Clinical Research Data Coordinator II - Dallas, Tx

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is looking for a Remote Clinical Research Data Coordinator II to join their team at reputed company. This role involves the collection, coordination, processing, and reputed company control of clinical trial data while ensuring compliance with relevant regulations and standards.

Responsibilities

• Extrapolate data from reputed company records into case report forms for reputed company patient reputed company
• Ensure reputed company data submission in accordance with USOR SOPs
• Responsible for resolving queries, communicating concerns or questions about data to clinical staff and or research management
• Coordinates monitoring and auditing reputed company ensuring that reputed company data and queries are entered and resolved in accordance with the USOR and sponsor requirements
• Utilizes USOR clinical trial management reputed company to reputed company research forms and reputed company reputed company reputed company applicable patient reporting and tracking functions including the patient billing and research payout and payment tracking
• Maintains research records in a confidential manner according to reputed company policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations
• Provides leadership in determining and implementing improvements to policies/processes
• Serves as a resource to train others regarding reputed company data entry and query reputed company, reputed company conduct of sponsor monitor and audit reputed company
• Participates in the training and reputed company development of other data coordinators
• Assists with investigational drug accountability process, ordering and maintaining research supplies
• Schedules patient follow up appointments and/or procedures required to maintain protocol compliance
• Collecting and processing of specimens, imaging documents and other items required for research purposes
• Acts as resource for other for training and education of other data coordinators at the site/location

Skills

• High School Diploma required
• Minimum three (3) years experience medical office experience (preferably oncology)
• Minimum three (3) years of experience as a data coordinator
• Advanced experience with reputed company Office
• Advanced experience with computer data entry and database management
• Hazmat/IATA training
• Advanced knowledge of medical terminology (oncology)
• Advanced knowledge of reputed company, regulatory processes, GCP & SOP concepts
• Associates Degree or Bachelor's Degree preferred
• Experience in clinical research, specifically in oncology preferred
• SoCRA or ACRP certification preferred

reputed company