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About the role
<p><strong><span data-contrast="auto">About Parabilis Medicines</span></strong><span data-ccp-props="{"134233117":false,"134233118":false,"201341983":0,"335551550":1,"335551620":1,"335559685":0,"335559737":0,"335559738":0,"335559739":0,"335559740":259}"> </span></p>
<p><span data-contrast="none">Parabilis Medicines is a clinical-stage biopharmaceutical company dedicated to creating extraordinary medicines for patients with serious diseases by unlocking biologically important targets long considered undruggable. The company has pioneered a new class of alpha-helical peptides – Helicons™ – capable of modulating intracellular proteins that have historically been beyond the reach of conventional medicines. The company’s lead investigational medicine, zolucatetide, is the first and only direct inhibitor of the β-catenin:TCF interaction, a central node in the Wnt/β-catenin pathway that has eluded drug developers for decades. Zolucatetide is being evaluated in the clinic across multiple Wnt/β-catenin-driven diseases, including desmoid tumors, familial adenomatous polyposis (FAP) and a range of other solid tumor indications. Beyond zolucatetide, Parabilis is advancing additional Helicon-based programs focused on other challenging targets where we believe our medicines could have life-altering impact. For more information, visit </span><a href="https://url.us.m.mimecastprotect.com/s/gYX5CkRVZgtkknDEuVhmcGHXzh?domain=parabilismed.com/"><span data-contrast="none"><span data-ccp-charstyle="Hyperlink">www.parabilismed.com</span></span></a><span data-contrast="none"> or follow us on </span><a href="https://url.us.m.mimecastprotect.com/s/7qd3ClYV50H11oWrFyinczUQak?domain=linkedin.com"><span data-contrast="none"><span data-ccp-charstyle="Hyperlink">LinkedIn</span></span></a><span data-contrast="none">.</span><span data-ccp-props="{"335551550":6,"335551620":6}"> </span></p>
<p><strong>What’s the opportunity?</strong></p>
<p>The Vice President of Biometry will lead Parabilis’s biometrics organization, overseeing biostatistics, statistical programming, data management, clinical data science and Real-World Data to support clinical development programs from early-phase through regulatory submission. This strategic role ensures the integrity, quality, and compliance of all clinical trial data and analyses while driving innovation in data strategy and statistical methodologies. Reporting to our SVP, Development Operations, the successful candidate will serve as a key member of the Development leadership team, partnering closely with Clinical Development, Clinical Operations, Regulatory Affairs, translational/computational biology and other functions to enable data-driven decision-making and successful product development.</p>
<ul>
<li>Lead and develop the Biometrics organization, including biostatistics, programming, data management Clinical Data science ensuring high-quality deliverables across all clinical programs and fostering a culture of scientific rigor, accountability, collaboration and innovation.</li>
<li>Oversee design and implementation of statistical methodologies for clinical trials.</li>
<li>Champion innovative methodologies, including adaptive and model-based approaches, to support efficient and agile drug development.</li>
<li>Provide strategic input into drug development strategies in collaboration with program-level and functional leadership, working closely with Clinical Development, Clinical Operations, and Translational Medicine.</li>
<li>Ensure the integrity, high quality and traceability of clinical trial data and the accuracy of all statistical analyses, leading to compliant deliverables in biometry.</li>
<li>Lead and support biometrics interactions with global health authorities.</li>
<li>Establish and maintain vendor partnerships ensuring quality and timely delivery of outsources biometrics activities.</li>
</ul>
<p><strong>What you’ll need to be successful:</strong></p>
<ul>
<li>Doctoral degree in Biostatistics or related field.</li>
<li>15+ years of biometrics experience within the biotech or pharmaceutical field.</li>
<li>Proven track record of leading, building, and managing teams.</li>
<li>Demonstrated record of fostering creativity, productivity, and execution with urgency, teamwork and accountability.</li>
<li>Company leader who leads by example, employs expertise and influence to encourage collaboration across departments, levels, and groups to achieve key objectives.</li>
<li>Deep knowledge of clinical trial design, regulatory requirements, and statistical environment.</li>
<li>Excellent problem-solving skills, strategic thinking, and ability to work in a fast-paced, collaborative environment.</li>
<li>Outstanding interpersonal skills, self-awareness, and ability to manage team dynamics.</li>
<li>Ideally, has worked in more than one therapeutic area and has direct experience with innovative Phase 1-3 clinical study designs for oncology.</li>
<li>Comfort with model-based drug development and agile drug development is important.</li>
<li>Appreciation for observational methodologies is preferred.</li>
<li>Ability to articulate complex methodologies to senior executives for their understanding is required with previous experience with presenting to senior executives being ideal.</li>
<li>Demonstrated use of AI tools in your current role and responsibilities is required. Advanced or innovated use of AI is a strong plus.</li>
</ul>
<p><strong>Core Values</strong></p>
<p>Parabilis is a team of passionate pioneers who are trailblazing the future of precision medicine with the aim of making a meaningful difference in the lives of patients. The company is committed to promoting an inspiring and flourishing working environment for all employees across the business, in all departments, and driving innovation for patient benefit.</p>
<ul>
<li><strong>Growth-Minded.</strong> We’re inventing a new class of medicines—one applicable to therapeutic targets that have been dreamt about, but always considered impossible to drug. Our work requires us to be curious, humble and adaptable.</li>
<li><strong>In(ter)dependent.</strong>We are fiercely <em>independent</em> as a leader in defying the limitations of current therapeutic modalities, and <em>interdependent</em> as a team as we work collaboratively to shift drug discovery paradigms and provide patients with better treatment options.</li>
<li><strong>Patient-focused.</strong>We are deeply focused on patient outcomes, and all energy in the company is focused on science as it translates to patient impact.</li>
<li><strong>All-In.</strong>We’re All-In on solving some of the hardest scientific challenges and delivering one of the most effective new classes of drugs in history.</li>
</ul>
<p>The base salary target for this position is $340,000-$380,000 per year, depending on experience, qualifications, and internal practices. Parabilis’s total compensation package also includes an annual target bonus, equity, and a comprehensive suite of competitive benefits designed to support our employees’ overall well-being.</p>
<p>As an equal opportunity employer, Parabilis values an inclusive workplace and welcomes applicants of all backgrounds and experiences. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors prohibited by law.</p>
<p><span style="font-weight: 400;"><span style="font-weight: 300;">30 Acorn Park Drive | Cambridge, MA 02140 | www.parabilismed.com</span></span></p>
Perks & benefits
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