Medical Science Liaison – Midwest

🔥 13 hours ago

🌽 Illinois, Iowa, +5 more states – Remote

🌽 Illinois – Remote 🌾 Iowa – Remote 🌾 Nebraska – Remote 🌾 North Dakota – Remote 🏰 Missouri – Remote 🗿 South Dakota – Remote 🧀 Wisconsin – Remote

💵 $196k - $239k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Secura Bio, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2019

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 $90M Debt Financing - Secura Bio on 2019-03

Healthcare • Manufacturing • Biotechnology

Secura Bio, Inc. is a commercial-stage biopharmaceutical company focused on developing, commercializing, and optimizing oncology therapies. The company emphasizes commercial strategy and market access for oncology medicines, supported by clinical development capabilities (clinical trials, expanded access, investigator-sponsored studies), medical education, and patient support programs. Headquartered in Berkeley Heights, New Jersey with an office in Dublin, Ireland, Secura Bio positions itself to maximize commercial outcomes for cancer treatments such as duvelisib.

📋 Description

• Identify, cultivate, and sustain relationships with key opinion leaders and healthcare professionals across the territory • Communicate scientific data, research concepts, and educational content about Secura Bio’s products and therapeutic focus • Set medical priorities, anticipate needs, and drive activities supporting Medical Affairs objectives • Deliver balanced, scientifically rigorous information about the pipeline and marketed products • Gather, synthesize, and communicate actionable field insights informing medical strategy, clinical development, and cross-functional decisions • Serve as a scientific resource during Medical Congresses, Advisory Boards, training programs, mentorship activities, and strategic planning meetings • Collaborate with Clinical Development and Operations on sponsored research, including site identification, evaluation, recruitment support, investigator engagement, external expert identification, and scientific collaboration management • Facilitate submission and review of investigator-initiated research proposals • Maintain investigator communications and support sponsored research activities • Partner with Market Development Managers and Key Account Managers on scientific education, customer support, and territory planning • Contribute to regional and national Medical Affairs strategies through territory planning, post-congress insights, and identification of emerging scientific trends • Adopt digital technologies to enhance scientific exchange, insight capture, and field effectiveness

🎯 Requirements

• Advanced degree strongly preferred (PharmD, PhD, MD) • Candidates with MBA/MSc require 5+ years of relevant experience • BA/BSc candidates require 8+ years of experience • Clinically licensed professionals (NP, PA, RN) may be considered with substantial oncology or Medical Affairs experience • Minimum of 3 years in Medical Affairs, field medical, pharmaceutical, or biotech roles • Strong subject matter expertise in oncology or hematology • Experience supporting product launches, understanding treatment paradigms, clinical pathways, and emerging research trends • Background in hematologic malignancies, especially lymphoma, preferred • Deep understanding of cancer biology, mechanisms of action, and therapeutic modalities relevant to rare lymphomas • Exceptional ability to communicate complex scientific information to oncologists, researchers, and multidisciplinary stakeholders • Proven capability to deliver scientific presentations to audiences of varying sizes • Ability to analyze complex clinical trial data and translate findings into clinically meaningful insights • Demonstrated experience engaging and building trust with key opinion leaders in oncology • Understanding of drug development and regulatory pathways • Knowledge of oncology practice patterns, care delivery models, and healthcare system dynamics • Ability to identify clinical research opportunities and evaluate investigator potential • Strong strategic thinking aligned with medical objectives • Ability to collaborate with clinical development, clinical operations, commercial, and Medical Affairs colleagues • Ability to work independently and deliver results in a fast-paced environment • Adaptability to evolving scientific data and shifting priorities • Familiarity with pharmaceutical and biotech compliance guidelines • Must reside within IL, ND, SD, NE, MO, IA, or WI, with preference for major metropolitan areas in IL, MN, or MO • Willingness to travel occasionally on weekends • Valid driver's license and good driving record

🏖️ Benefits

• Flexibility to travel 60-80% of the time • Attendance at major oncology conferences such as ASCO, ASH, and SOHO, as well as regional conferences • Willingness and flexibility to travel occasionally on weekends for meetings and conferences • Valid driver's license and good driving record