Clinical Research Scientist - VahatiCor

<p>Title: Clinical Research Scientist </p><p>Status: Exempt</p><p>Location: Onsite San Clara, CA </p><p>Reports to: Vice President of Clinical Affairs</p><p></p><p><strong>About the Company </strong></p><p>VahatiCor is developing next-generation intravascular technologies designed to improve outcomes in cardiovascular care. As an early-stage company, we are building clinical and regulatory strategy from the ground up to support product development, approval, and adoption.<br><br></p><p><strong>The Role</strong><br>The Clinical Research Scientist will support clinical evidence generation and study design, working closely with cross-functional teams to help develop the data needed for regulatory approval and clinical adoption. This role focuses on contributing to clinical study planning, interpreting data, and developing scientific and regulatory documentation. It is not a clinical operations role, but rather a partner to clinical and regulatory teams in shaping and supporting evidence development.</p><p><br><strong>What You’ll Do</strong></p><p><br><em>Clinical Trial Design &amp; Support</em></p><ul><li>Support the design of clinical trial protocols aligned with pre- and post-market evidence needs</li><li>Contribute to defining endpoints, patient populations, and success metrics</li><li>Partner with cross-functional teams to ensure studies are feasible and aligned with development timelines</li><li>Support study planning, including site strategy, sample size considerations, and data collection approach</li><li>Ensure studies are structured to support regulatory submissions and clinical adoption</li></ul><p></p><p><em>Clinical Evidence Generation &amp; Data Interpretation</em></p><ul><li>Interpret clinical data to assess safety, efficacy, and clinical relevance </li><li>Partner with statisticians to develop and execute analysis plans</li><li>Develop manuscripts, abstracts, and presentations to communicate findings</li><li>Collaborate with Key Opinion Leaders (KOLs) to generate scientific insight<br> </li></ul><p></p><p><strong>Regulatory Support &amp; Compliance</strong></p><ul><li>Translate clinical data into regulatory documentation (e.g., protocols, CERs, clinical<br>sections of submissions)</li><li>Ensure clinical evidence supports regulatory filings, marketing authorization, and post-<br>market activities</li><li>Support regulatory discussions and alignment between clinical and regulatory strategy</li><li>Ensure compliance with global clinical and regulatory requirements<br></li></ul><p></p><p><em>Cross-Functional Relationships</em></p><ul><li>Work with R&amp;D, Regulatory, and external advisors to support clinical activities</li><li>Contribute to ongoing clinical efforts in a fast-moving, early-stage environment</li></ul><p></p><p><strong>What You Bring</strong></p><ul><li>Advanced degree (MD, PhD, or MS) and 5+ years of clinical research experience in the medical device industry (cardiovascular preferred) </li><li>Demonstrated experience designing clinical studies (not just executing them)</li><li>Strong scientific writing skills with experience developing protocols, reports, and manuscripts</li><li>Ability to interpret complex clinical data and translate it into clear, actionable insights</li><li>Strong communication skills with the ability to engage physicians, internal teams, and external stakeholders<br> <br> </li></ul><p><strong>Eligibility</strong></p><p>Candidates must be permanently authorized to work in the United States without the need for<br>current or future visa sponsorship. We are currently unable to sponsor employment visas, or<br>permanent residency (PERM) applications.</p><p></p><p><br><strong>Location and Compensation</strong> </p><p>This is an onsite role based in Santa Clara, CA, and is open to candidates living within a<br>reasonable commuting distance of our office. At this time, we are not considering applicants<br>who would need to relocate, either within or outside of California. There is no relocation<br>package available.</p><p><br>T45 and VahatiCor are committed to fair and equitable pay practices and may also consider additional<br>compensation elements such as bonuses, equity, and benefits as part of the total rewards<br>package.</p><p><br>Salary ranges are based on San Francisco Bay Area market data. Actual compensation offered<br>may vary depending on factors such as experience, skills, qualifications, and abilities relevant to<br>the role, as well as the geographic location of the individual hired.</p><p><br>The anticipated salary range for this position is $144,000 - $195,000 annually, based on San<br>Francisco Bay Area market data. Most candidates should expect to receive an offer at the mid-point of the range. </p><p><br>Willingness to travel on occasion.</p><p></p><p><br><strong>Equal Employment Opportunity</strong></p><p>VahatiCor is an Equal Opportunity Employer. We are committed to building a diverse and<br>inclusive workplace and do not discriminate based on race, color, religion, sex, sexual<br>orientation, gender identity, national origin, disability, veteran status, or any other legally<br>protected status.</p><p></p><p><strong>Third-Party Recruiter Notice</strong></p><p>VahatiCor does not accept unsolicited resumes from agencies. Any resumes submitted without<br>a signed agreement will be considered the property of T45 Labs and VahatiCor and no fees will<br>be paid. Agencies interested in submitting candidates may email careers@t45labs.com</p><p></p><p></p><p></p><p></p>