Clinical Trial Associate - Contractor, Hybrid in Office

Clinical Trial Associate - Contractor, Hybrid in OfficeOverviewJasper 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.ResponsibilitiesAssist in the development of trial-related documents, including protocols, informed consent forms, case report forms, and study manualsCoordinate with cross-functional teams to ensure timely availability of trial supplies, investigational products, and study materialsResponsible for agendas and minutes for assigned Study Execution Team MeetingsSupport the implementation and management of clinical trials according to study protocols, standard operating procedures (SOPs), and regulatory requirementsTrack and manage study-related documentation, including regulatory submissions, ethics committee approvals, and site contractsResponsible for internal team training tracking and compliancePerform data review and data cleaning activities, ensuring accuracy and completeness of study dataAssist in the review and reconciliation of clinical trial data, identifying and resolving discrepanciesReview CRO trip reports for completeness and accuracySupport the maintenance of trial master files, ensuring completeness and accuracy of essential documents through routine QCResponsible for sample management tracking and shipment coordinationQualifications and ExperienceBachelor/'s degree in a scientific or healthcare-related field1-2 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 requirementsFamiliarity with clinical trial protocols, informed consent processes, and data collection methodsStrong organizational skills and attention to detailExcellent written and verbal communication skillsProficiency in using clinical trial management systems and electronic data capture systemsAbility to work independently and collaboratively in a team environmentAdditional InformationSeniority level: Not ApplicableEmployment type: Full-timeJob function: Research, Analyst, and Information TechnologyIndustries: Transportation, Logistics, Supply Chain and StorageReferrals increase your chances of interviewing at Jasper Therapeutics by 2xGet notified about new Clinical Trial Associate jobs in Redwood City, CA.San Francisco Bay Area $87,000.00-$104,000.00 7 hours agoSimilar rolesClinical Research Coordinator to Home-Based CRA (Clinical Research Associate) - Alameda, CA $79,500.00-$138,700.00 6 days agoClinical Research Associate/Senior Clinical Research Associate - Alameda, CA $72,100.00-$114,700.00 5 days agoResearch Associate, Molecular Development - San Francisco, CA $90,000.00-$100,000.00 1 month agoClinical Research Assistant - Health Educator - San Francisco, CA $26.76-$35.45 1 month agoAssistant Clinical Research Coordinator (Hybrid Opportunity)Clinical Trial Associate II (Contractor)We're unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr

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