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Job description
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.
Responsibilities
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
Qualifications and Experience
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
Additional Information
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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Assistant Clinical Research Coordinator (Hybrid Opportunity)
Clinical Trial Associate II (Contractor)
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Worksite address
redwood city, CA, 94061, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.