Senior Clinical Trial Manager

BioPhase Solutions specializes in recruiting top talented professionals for the San Diego County Scientific community. We are currently looking for an ONSITE Sr. Clinical Trial Manager to work for a leading San Diego biotech company.*Must be local and willing to work onsite in San Diego, CA.ResponsibilitiesLead day-to-day clinical operations activities for assigned studies, ensuring execution aligns with timelines, budget, and quality expectationsOversee external vendors and CRO partners to ensure efficient and compliant study conductSupport study planning activities, including development of key operational documents (e.g., monitoring plans, enrollment strategies, study manuals)Track and analyze study metrics (e.g., site performance, data quality, enrollment progress) and escalate risks or issues as neededPartner cross-functionally with Clinical, Data Management, Regulatory, Safety, and other teams to support study executionReview study documentation including monitoring reports, protocol deviations, and data listings to ensure quality and complianceContribute to development of study materials such as informed consent forms, CRFs, and site-facing documentationSupport site selection and feasibility assessments, including evaluation of investigators and site capabilitiesAssist with clinical trial agreements, budgets, and vendor oversight in collaboration with internal stakeholdersEnsure proper documentation and maintenance of Trial Master File (TMF) in accordance with regulatory requirementsParticipate in study team meetings and provide updates on study progress, risks, and timelinesSupport preparation of clinical study reports and resolution of data-related queriesProvide guidance and support to CRAs and other study team members as neededQualificationsBachelor’s or Master’s degree in a life sciences or related field5+ years of experience in clinical trial management and/or monitoring within biotech or pharmaceutical environmentsExperience supporting Phase I–III clinical studiesStrong knowledge of ICH-GCP guidelines and global regulatory requirementsExperience managing CROs and external vendorsFamiliarity with clinical systems such as EDC, CTMS, and IRT platformsAbility to manage multiple priorities and work effectively in a fast-paced environmentStrong organizational, problem-solving, and communication skillsExperience working across global teams and time zones is preferredPrior experience in small to mid-sized biotech companies is a plusWillingness to travel as neededWhat we offer:As we work to develop innovations that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.· Full support and career-development resources to help you reach your potential· A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and actApply now and let's make work better!www.biophaseinc.com