Clinical Data Manager - T45 Labs
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T45 Labs
Santa Clara, CA (In Person)
Full-Time
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Job Description
Clinical Data Manager
- T45 Labs T45 Labs Santa Clara, CA Job Details Full-time $117
- $159 a day 1 day ago Qualifications Power BI Data visualization software proficiency Computer Science Configuration management Process improvement Data reporting Clinical trial projects Tableau Databases System maintenance Analysis skills ICH guidelines Clinical research compliance Bachelor's degree Data quality monitoring Smartsheet TIBCO Spotfire JMP Data validation Senior level Cross-functional collaboration Bachelor's degree in computer science Cross-functional communication FDA regulations Full Job Description Clinical Data Manager•T45
Labs Status:
Full-time, Exempt Location:
Onsite, Santa Clara, CA Reports to: Sr. Clinical Trials Manager About the Company T45 Labs advances breakthrough cardiovascular technologies from early development into the clinic. We focus on selecting the right innovations, developing them with precision, and moving them through critical clinical and regulatory milestones so they reach the physicians and patients who need them most. About the Role We are seeking a Clinical Data Manager to lead data management activities across multiple medical device clinical programs. This is a hands-on role responsible for managing and maintaining clinical data systems to ensure accuracy, integrity, and usability of study data. You will work closely with Clinical Operations, Biostatistics, and external partners to support studies from early feasibility through pivotal trials. This role is well-suited for someone who is detail-oriented, technically strong, and comfortable operating in a fast-paced, start-up environment where priorities evolve and execution matters Key Responsibilities Develop and maintain Data Management Plans (DMPs) across clinical studies Design Case Report Forms (CRFs) aligned with study protocols Configure and manage CRFs within Electronic Data Capture (EDC) systems Perform ongoing data cleaning, validation, and discrepancy management Generate, track, and resolve data queries; identify trends and inconsistencies Lead study-level database lock activities, including query closure and documentation review Conduct regular data review and reconciliation to maintain database integrity Partner with Clinical Operations, Biostatistics, and Regulatory teams to ensure data quality and compliance Provide data listings, reports, and study metrics to support clinical teams Build and maintain study trackers using Excel and/or Smartsheet to monitor progress and data quality Apply formulas, filters, and logic functions to ensure accuracy and visibility of study data Support process improvement initiatives to enhance data workflows and reporting Required Experience and Qualifications Bachelor's degree in Life Sciences, Computer Science, or a related field 5+ years of experience in clinical data management, preferably in a medical device environment Hands-on experience with EDC systems and CRF configuration Strong knowledge of GCP, FDA, and ICH guidelines related to clinical data management Experience with data cleaning, query management, and database lock processes Strong analytical and problem-solving skills with high attention to detail Proficiency in Excel and/or Smartsheet for tracking and data organization Ability to work cross-functionally and manage multiple priorities in a fast-paced, start-up environment Preferred Qualifications Experience supporting cardiovascular or catheter-based medical device studies Familiarity with EDC configuration and ongoing system management (not initial build) Familiarity with data visualization tools (e.g., Power BI, Tableau, Spotfire, JMP) Experience supporting early feasibility or first-in-human studies What We're Looking For A hands-on data manager who takes ownership of data quality and keeps studies moving Strong attention to detail with the ability to identify inconsistencies and resolve issues proactively Comfortable working across multiple studies and shifting priorities in a fast-paced, start-up environment Able to work independently while collaborating closely with Clinical Operations, Biostatistics, and external partners Practical, execution-focused, and responsive to the needs of evolving clinical programs. Eligibility Candidates must be permanently authorized to work in the United States without the need for current or future visa sponsorship. We are currently unable to sponsor employment visas, or permanent residency (PERM) applications. Location and Compensation This is an onsite role based in Santa Clara, CA, and is open to candidates living within a reasonable commuting distance of our office. At this time, we are not considering applicants who would need to relocate, either within or outside of California. There is no relocation package available. T45 Labs is committed to fair and equitable pay practices and may also consider additional compensation elements such as bonuses, equity, and benefits as part of the total rewards package. Salary ranges are based on San Francisco Bay Area market data. Actual compensation offered may vary depending on factors such as experience, skills, qualifications, and abilities relevant to the role, as well as the geographic location of the individual hired. The anticipated salary range of this position is $117- $159 annually, based on San Francisco Bay Area market data.
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