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.
The Role 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.
What Youll Do
Clinical Trial Design & Support
Support the design of clinical trial protocols aligned with pre- and post-market evidence needs
Contribute to defining endpoints patient populations and success metrics
Partner with cross-functional teams to ensure studies are feasible and aligned with development timelines
Support study planning including site strategy sample size considerations and data collection approach
Ensure studies are structured to support regulatory submissions and clinical adoption
Clinical Evidence Generation & Data Interpretation
Interpret clinical data to assess safety efficacy and clinical relevance
Partner with statisticians to develop and execute analysis plans
Develop manuscripts abstracts and presentations to communicate findings
Collaborate with Key Opinion Leaders (KOLs) to generate scientific insight
Regulatory Support & Compliance
Translate clinical data into regulatory documentation (e.g. protocols CERs clinical sections of submissions)
Support regulatory discussions and alignment between clinical and regulatory strategy
Ensure compliance with global clinical and regulatory requirements
Cross-Functional Relationships
Work with R&D Regulatory and external advisors to support clinical activities
Contribute to ongoing clinical efforts in a fast-moving early-stage environment
What You Bring
Advanced degree (MD PhD or MS) and 5 years of clinical research experience in the medical device industry (cardiovascular preferred)
Demonstrated experience designing clinical studies (not just executing them)
Strong scientific writing skills with experience developing protocols reports and manuscripts
Ability to interpret complex clinical data and translate it into clear actionable insights
Strong communication skills with the ability to engage physicians internal teams and external stakeholders
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 and VahatiCor are 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 for this position is $144000 - $195000 annually based on San Francisco Bay Area market data. Most candidates should expect to receive an offer at the mid-point of the range.
Willingness to travel on occasion.
Equal Employment Opportunity
VahatiCor is an Equal Opportunity Employer. We are committed to building a diverse and inclusive workplace and do not discriminate based on race color religion sex sexual orientation gender identity national origin disability veteran status or any other legally protected status.
Third-Party Recruiter Notice
VahatiCor does not accept unsolicited resumes from agencies. Any resumes submitted without a signed agreement will be considered the property of T45 Labs and VahatiCor and no fees will be paid. Agencies interested in submitting candidates may email
Required Experience:
IC
DescriptionTitle: Clinical Research Scientist Status: ExemptLocation: Onsite San Clara CA Reports to: Vice President of Clinical AffairsAbout the Company VahatiCor is developing next-generation intravascular technologies designed to improve outcomes in cardiovascular care. As an early-stage company ...
Description
Title: Clinical Research Scientist
Status: Exempt
Location: Onsite San Clara CA
Reports to: Vice President of Clinical Affairs
About the Company
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.
The Role 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.
What Youll Do
Clinical Trial Design & Support
Support the design of clinical trial protocols aligned with pre- and post-market evidence needs
Contribute to defining endpoints patient populations and success metrics
Partner with cross-functional teams to ensure studies are feasible and aligned with development timelines
Support study planning including site strategy sample size considerations and data collection approach
Ensure studies are structured to support regulatory submissions and clinical adoption
Clinical Evidence Generation & Data Interpretation
Interpret clinical data to assess safety efficacy and clinical relevance
Partner with statisticians to develop and execute analysis plans
Develop manuscripts abstracts and presentations to communicate findings
Collaborate with Key Opinion Leaders (KOLs) to generate scientific insight
Regulatory Support & Compliance
Translate clinical data into regulatory documentation (e.g. protocols CERs clinical sections of submissions)
Support regulatory discussions and alignment between clinical and regulatory strategy
Ensure compliance with global clinical and regulatory requirements
Cross-Functional Relationships
Work with R&D Regulatory and external advisors to support clinical activities
Contribute to ongoing clinical efforts in a fast-moving early-stage environment
What You Bring
Advanced degree (MD PhD or MS) and 5 years of clinical research experience in the medical device industry (cardiovascular preferred)
Demonstrated experience designing clinical studies (not just executing them)
Strong scientific writing skills with experience developing protocols reports and manuscripts
Ability to interpret complex clinical data and translate it into clear actionable insights
Strong communication skills with the ability to engage physicians internal teams and external stakeholders
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 and VahatiCor are 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 for this position is $144000 - $195000 annually based on San Francisco Bay Area market data. Most candidates should expect to receive an offer at the mid-point of the range.
Willingness to travel on occasion.
Equal Employment Opportunity
VahatiCor is an Equal Opportunity Employer. We are committed to building a diverse and inclusive workplace and do not discriminate based on race color religion sex sexual orientation gender identity national origin disability veteran status or any other legally protected status.
Third-Party Recruiter Notice
VahatiCor does not accept unsolicited resumes from agencies. Any resumes submitted without a signed agreement will be considered the property of T45 Labs and VahatiCor and no fees will be paid. Agencies interested in submitting candidates may email