Executive / Senior Medical Director, Clinical Development

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    "location": {
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      "state": "Massachusetts",
      "postalCode": "02101",
      "addressCountry": "United States"
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    "datePosted": "2026-03-09",
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    "description": "<p><span> </span></p>\n<p><span style=\"font-weight: bold\"><span><span>Summary:</span></span></span><span> </span></p>\n<p><span><span>We are looking for a</span><span>n</span><span> </span><span>Executive / </span><span>Senior</span><span> </span><span>Medical </span><span>Director</span><span> (</span><span>l</span><span>eve</span><span>l</span><span> dependent on qualifications)</span><span> to support our growing Clinical Development team! Reporting to the </span><span>Vice President </span><span>of Clinical Development. The position provides </span><span>medical</span><span> and</span><span> scientific</span><span> leadership</span><span> for </span><span>Verastem’s</span><span> potentially best-in-class</span><span> KRAS G12D ON/OFF inhibitor</span><span>:</span><span> VS-7375 </span><span>P</span><span>rogram. This individual </span><span>will </span><span>serve as the Clinical Lead</span><span> </span><span>for</span><span> one or more studies to</span><span> lead</span><span> study execution</span><span> and</span><span> development strateg</span><span>y</span><span>, as well as</span><span> being</span><span> </span><span>a key member of</span><span> the </span><span>Program Team</span><span> to </span><span>bring VS-7375 </span><span>through development cycles</span><span> and potential</span><span> market authorization application</span><span>s</span><span>.</span></span><span> </span></p>\n<p><span> <br></span><span style=\"font-weight: bold\"><span><span>Responsibilities</span></span></span><span> </span></p>\n<ul>\n<li><span><span>Support</span><span>s</span><span> the design and execution of assigned clinical trial</span><span>(s)</span><span> and works closely </span><span>with </span><span>cross functional study team members to execute activities associated with the conduct of the clinical trials. </span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Serves as the p</span><span>rimary medical / safety contact for assigned clinical trials, ensuring </span><span>compliance </span><span>and </span><span>patient safety.</span><span> </span><span>Serve as the primary contact for medical-related inquiries from investigators, regulatory agencies, and internal/external teams, ensuring consistent protocol interpretation and clarification</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Partner</span><span>s</span><span> with Clinical Science</span><span>, </span><span>Data Management</span><span>, Sta</span><span>tistical</span><span> Programing to </span><span>ensure data integrity</span><span>.</span><span> </span><span>L</span><span>ead regular data reviews</span><span> and insight generation to </span><span>guide development </span><span>strategy</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Collaborate</span><span>s</span><span> with </span><span>S</span><span>afety on </span><span>reporting of </span><span>identified</span><span> adverse events (AEs), serious adverse events (SAEs), and other safety-related events.</span><span> </span><span>Contributes to </span><span>safety profile characterization</span><span> and </span><span>corresponding risk mitigation </span><span>strategy / plans</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>A</span><span>c</span><span>t</span><span>s</span><span> as a key member of the Program Team</span><span> to </span><span>devise integrated development plan(s)</span><span> and</span><span> development</span><span> </span><span>/</span><span> </span><span>regulatory strategies. </span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Author</span><span>s</span><span> and </span><span>develop</span><span> key study and regulatory documents with the cross functional team, including, but not limited to study protocol, investigator brochure, informed consent form, and clinical study reports. Contribute</span><span>s</span><span> to scientific publications, including conference abstracts and peer-reviewed journal articles. </span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Represent</span><span>s</span><span> the study / program</span><span> and</span><span> i</span><span>nteract</span><span>s</span><span> on a regular basis with key internal</span><span> / </span><span>external partners and stakeholders, including key opinion leaders, clinical investigators, clinicians, scientists as well as </span><span>internal leadership team</span><span> and R&amp;D</span><span>.</span><span> L</span><span>ead and present at</span><span> investigator meetings and advisory</span><span> committees.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Maintains scientific and clinical knowledge in </span><span>oncology and provides input on </span><span>Verastem’s</span><span> pipeline, translational and preclinical </span><span>work.</span></span><span> </span></li>\n</ul>\n<p><span> </span></p>\n<p><span style=\"font-weight: bold\"><span><span>Required qualifications</span></span></span><span> </span></p>\n<ul>\n<li><span><span> Medical Degree</span><span> (M.D. or equivalent)</span><span> </span><span>required</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><br><span>5</span><span>+ </span><span>years</span><span> of </span><span>experience</span><span> in </span><span>biotech / pharma </span><span>industry o</span><span>ncology</span><span> drug development</span><span> </span><span>(</span><span>or</span><span> substantial</span><span> </span><span>investigational therapeutics</span><span> experience as a clinical investigator </span><span>if </span><span>not meeting </span><span>industry</span><span> experience</span><span> </span><span>requirement</span><span>)</span><span> </span><span>is </span><span>required</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Knowledge of Good Clinical Practices (</span><span>cGCP</span><span>); comprehensive knowledge of clinical trial design; understanding of the overall global drug development process.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Knowledge of current external regulatory environment, </span><span>e.g.</span><span> FDA, EMA requirements</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Ability to work independently and the exercise of good medical, clinical judgment in resolving critical problems not always covered by existing standards, </span><span>policies</span><span> and procedures.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Excellent</span><span> interpersonal, verbal </span><span>communication,</span><span> and influencing skills.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>A track record</span><span> of leading cross-functional matrix teams.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Demonstrated ability to develop and cultivate relationships with key internal, and external, partners and stakeholders.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>S</span><span>trong analytical and presentation skills: effective at summarizing and presenting the key considerations and decision-points.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Comfortable working in fast paced entrepreneurial environment, with a flexible mindset to be successful in a biotech corporate culture</span><span>.</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Ability to travel up to 20% of the </span><span>time.</span></span><span> </span></li>\n</ul>\n<p><span> </span></p>\n<p><span style=\"font-weight: bold\"><span><span>Preferred</span><span> qualifications</span></span></span><span> </span></p>\n<ul>\n<li><span><span>Board-certified in oncology</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>Experience in GI oncology and/or lung cancer</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>With </span><span>an </span><span>established </span><span>investigator / KOL network in oncology</span></span><span> </span></li>\n</ul>\n<ul>\n<li><span><span>NDA / BLA experience</span></span><span> </span></li>\n</ul>",
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