FULL-TIME
Posted Oct 6, 2026
Job Description
About Riboscience 🧬
Riboscience is a clinical-stage biotechnology company developing innovative treatments for serious infectious diseases and cancer. We leverage ribose and structure-guided design technologies to discover medicines that target proteins essential to infectious pathogens, tumor cells, and the anti-tumor immune response.
About the Role:
As a Clinical Trial Manager, you will play a critical role in our clinical operations by overseeing the day-to-day management of one or more clinical trials. You’ll collaborate with cross-functional stakeholders, manage study deliverables, ensure the highest level of data quality, and provide guidance to Clinical Research Associates and Clinical Trial Associates.
Key Responsibilities:
• Manage day-to-day execution of one or more clinical studies under the direction of senior Clinical Operations leadership.
• Ensure studies are conducted in compliance with protocol, ICH-GCP, FDA, and applicable regulatory requirements.
• Track study timelines, milestones, and performance metrics.
• Coordinate development and review of study documents, including protocols, informed consent forms, CRFs, study plans, investigator brochures, and clinical study reports.
• Oversee CROs and vendors, including selection, contracting support, performance monitoring, and issue resolution.
• Provide oversight and guidance to CRAs and Clinical Trial Associates.
• Monitor site performance and build strong relationships with investigators and study coordinators.
• Identify operational risks and implement mitigation strategies.
• Oversee Trial Master File (TMF) quality and completeness.
• Collaborate with cross-functional teams including Clinical Development, Data Management, Biostatistics, Regulatory Affairs, and Medical Writing.
Qualifications:
• Bachelor's degree in Life Sciences or related field (Master's preferred).
• 5+ years of clinical research experience with at least 2 years as a Clinical Trial Manager.
• Experience managing Phase II and/or Phase III clinical trials.
• Experience working with CROs and external vendors.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial operations.
• Excellent project management and communication skills.
• Experience working in biotechnology or pharmaceutical industry.
• Ability to thrive in a fast-paced startup environment.
📩 How to Apply:
Please send your cover letter and CV directly to careers@riboscience.com.
Learn more about the role and our science here: https://www.riboscience.com/job-details-3
#ClinicalTrialManager #ClinicalOperations #OncologyTrials #BiotechJobs #PharmaJobs #SFBayAreaJobs #Riboscience #LifeSciences #ClinicalResearch
Riboscience is a clinical-stage biotechnology company developing innovative treatments for serious infectious diseases and cancer. We leverage ribose and structure-guided design technologies to discover medicines that target proteins essential to infectious pathogens, tumor cells, and the anti-tumor immune response.
About the Role:
As a Clinical Trial Manager, you will play a critical role in our clinical operations by overseeing the day-to-day management of one or more clinical trials. You’ll collaborate with cross-functional stakeholders, manage study deliverables, ensure the highest level of data quality, and provide guidance to Clinical Research Associates and Clinical Trial Associates.
Key Responsibilities:
• Manage day-to-day execution of one or more clinical studies under the direction of senior Clinical Operations leadership.
• Ensure studies are conducted in compliance with protocol, ICH-GCP, FDA, and applicable regulatory requirements.
• Track study timelines, milestones, and performance metrics.
• Coordinate development and review of study documents, including protocols, informed consent forms, CRFs, study plans, investigator brochures, and clinical study reports.
• Oversee CROs and vendors, including selection, contracting support, performance monitoring, and issue resolution.
• Provide oversight and guidance to CRAs and Clinical Trial Associates.
• Monitor site performance and build strong relationships with investigators and study coordinators.
• Identify operational risks and implement mitigation strategies.
• Oversee Trial Master File (TMF) quality and completeness.
• Collaborate with cross-functional teams including Clinical Development, Data Management, Biostatistics, Regulatory Affairs, and Medical Writing.
Qualifications:
• Bachelor's degree in Life Sciences or related field (Master's preferred).
• 5+ years of clinical research experience with at least 2 years as a Clinical Trial Manager.
• Experience managing Phase II and/or Phase III clinical trials.
• Experience working with CROs and external vendors.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial operations.
• Excellent project management and communication skills.
• Experience working in biotechnology or pharmaceutical industry.
• Ability to thrive in a fast-paced startup environment.
📩 How to Apply:
Please send your cover letter and CV directly to careers@riboscience.com.
Learn more about the role and our science here: https://www.riboscience.com/job-details-3
#ClinicalTrialManager #ClinicalOperations #OncologyTrials #BiotechJobs #PharmaJobs #SFBayAreaJobs #Riboscience #LifeSciences #ClinicalResearch
Additional Details
- City
- Palo Alto
- State
- California
- Country
- US
Apply and matching require a free OVN account. Browse listings anytime without signing in.