Clinical Trial Associate – Contractor, Hybrid in Office

Clinical Trial Associate – Contractor, Hybrid in Office Overview

Jasper is a biotechnology company focused on developing new therapies to treat both chronic and life-threatening diseases. Our mission is to make safer and potentially curative therapy possible for more patients in need. We are bringing together a team of high performing biotech professionals, leading academic institutions and a strong syndicate of healthcare-focused investors to achieve our vision.

Position Summary: Reporting to a Sr Clinical Trial Manager, the Clinical Trial Associate (CTA) plays a crucial role in supporting the planning, execution, and management of clinical trials within a small biotech company. The CTA works closely with the clinical operations team to ensure the successful implementation of clinical trials, adherence to regulatory guidelines, and the collection of high-quality data. This position requires strong organizational skills, attention to detail, and the ability to work effectively in a fast-paced and dynamic environment.

This position will be a hybrid role requiring 2-3 days in the office.

• Assist in the development of trial-related documents, including protocols, informed consent forms, case report forms, and study manuals
• Coordinate with cross-functional teams to ensure timely availability of trial supplies, investigational products, and study materials
• Responsible for agendas and minutes for assigned Study Execution Team Meetings
• Support the implementation and management of clinical trials according to study protocols, standard operating procedures (SOPs), and regulatory requirements
• Track and manage study-related documentation, including regulatory submissions, ethics committee approvals, and site contracts
• Responsible for internal team training tracking and compliance
• Perform data review and data cleaning activities, ensuring accuracy and completeness of study data
• Assist in the review and reconciliation of clinical trial data, identifying and resolving discrepancies
• Review CRO trip reports for completeness and accuracy
• Support the maintenance of trial master files, ensuring completeness and accuracy of essential documents through routine QC
• Responsible for sample management tracking and shipment coordination

• Bachelor s degree in a scientific or healthcare-related field
• 1-2 years prior experience in clinical research, preferably as a Clinical Trial Assistant or in a similar role;
  Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
• Familiarity with clinical trial protocols, informed consent processes, and data collection methods
• Strong organizational skills and attention to detail
• Excellent written and verbal communication skills
• Proficiency in using clinical trial management systems and electronic data capture systems
• Ability to work independently and collaboratively in a team environment

• Seniority level:
  Not Applicable
• Employment type:
  
  Full-time
• Job function:
  Research, Analyst, and Information Technology
• Industries:
  Transportation, Logistics, Supply Chain and Storage

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