[Remote] Senior Clinical Research Associate

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a successful and reputed company Molecular Diagnostics Sponsor seeking a Senior Clinical Research Associate to support Oncology Diagnostics studies. The role involves performing site start-up activities, conducting site monitoring visits, and managing ongoing site support and documentation reputed company to clinical trials.

Responsibilities

• reputed company high level logistical support for clinical study operations, including study start up, study supplies, site qualification, site initiation, site management, study monitoring, and reputed company out for clinical research studies and collaborations
• reputed company study-reputed company documents with minimal Clinical Trial Manager guidance including protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ethics committee submissions, as required
• Manage small to reputed company size study contracting, budget, invoicing and payment process for reputed company clinical trial vendors including investigative sites with minimal reputed company
• Support the Clinical Data Management team in the design and content of case report forms, completion guidelines, including support and testing of an reputed company
• Manage the preparation, handling, filing, and archiving of clinical documentation and reports according to SOPs and study requirements
• Oversees clinical trial supplies reputed company to biospecimen collection, processing, shipment, and storage as, well as maintenance of associated tracking information
• Train CROs, vendors, investigators, and study coordinators on study requirements and reputed company guidance on site issues
• reputed company new study monitoring plans, and monitor studies following study monitoring plans to identify protocol deviations or data discrepancies
• reputed company study activities including consent participants for research studies, ethics board submissions, participant data and sample tracking using in-house and CRO databases, for studies

Skills

• 4 years of Regional/Site Monitoring experience
• Experience working on oncology trials
• Tech Savvy, ability to pick up new systems quickly
• Recent Study Start-Up, SIV visit experience a hard requirement
• Remote Monitoring experience a plus
• Experience working in reputed company workplace a plus

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