
51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
💰 $25M Post-IPO Equity on 2022-04
Biotechnology • Pharmaceuticals • Healthcare
Zentalis Pharmaceuticals is developing potentially best-in-class, novel small molecules that target fundamental biological pathways in cancer. The company focuses on creating therapeutics aimed at treating various forms of cancer by leveraging innovative approaches in biotechnology.
🕒 August 7
Where this job comes from
Posted on Zentalis Pharmaceuticals's careers page, not through a job board
First seen by Remote Rocketship August 7
Still open on Zentalis Pharmaceuticals's site. Checked 1 hour ago.

51 - 200 employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
💰 $25M Post-IPO Equity on 2022-04
Biotechnology • Pharmaceuticals • Healthcare
Zentalis Pharmaceuticals is developing potentially best-in-class, novel small molecules that target fundamental biological pathways in cancer. The company focuses on creating therapeutics aimed at treating various forms of cancer by leveraging innovative approaches in biotechnology.
• Develop and maintain long-term, strategic scientific relationships with key opinion leaders, investigators, advanced practice providers, pharmacists, and other healthcare professionals • Develop and execute strategic engagement plans for key opinion leaders, investigators, and priority accounts within the assigned territory • Identify new investigators, sites, and scientific engagement opportunities • Conduct fair-balanced, non-promotional scientific exchange and deliver scientific presentations and medical education to healthcare professionals • Interpret and communicate complex clinical and scientific data accurately for the audience’s knowledge and needs • Identify, analyze, document, and communicate actionable medical insights and competitive intelligence • Support local, regional, and national scientific meetings through key opinion leader engagement, scientific exchange, insight gathering, and congress coverage • Collaborate with Clinical Development, Clinical Operations, Translational Medicine, Medical Communications, Regulatory, and other internal teams • Provide scientific support for clinical development and research activities, including strategic engagement with investigators and clinical trial sites • Engage in scientific discussions regarding disease-state biomarkers, clinical relevance, and patient identification for ongoing clinical trials • Support or lead planning and execution of local, regional, and national scientific advisory boards • Serve as the Medical Affairs liaison for assigned investigator-sponsored trials (ISTs) • Lead assigned Field Medical projects and contribute to broader team initiatives • Maintain scientific and therapeutic-area expertise through professional development, review of emerging clinical data, and awareness of the evolving treatment landscape • Maintain accurate and timely documentation of field activities • Communicate effectively with all levels of the organization and external stakeholders
• Master’s degree or advanced clinical/scientific degree (PharmD, PhD, MD, DO, NP, PA) required • Minimum of 5 years of biotechnology, pharmaceutical, or related life sciences experience • At least 3 years as an MSL or in a comparable Field Medical role • Oncology experience strongly preferred • Ability to independently interpret and communicate complex scientific and clinical data accurately, clearly, and in a balanced, evidence-based manner • Strong presentation and interpersonal skills • Ability to establish and maintain credible scientific relationships with key opinion leaders, investigators, and other healthcare professionals • Ability to independently develop and execute strategic engagement plans aligned with Field Medical strategy and priorities • Strong working knowledge of GCP, FDA regulations, Medical Affairs compliance requirements, and applicable industry guidelines • Strong organizational skills and ability to work independently while collaborating effectively within a cross-functional team • Requires up to 60% regional travel and limited international travel • Must hold a valid driver’s license and be able to safely operate a vehicle to travel to clinical sites for investigator visits • Proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint
• Up to 60% regional travel and limited international travel
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