Serve as a field-based scientific resource and trusted exchange partner for key opinion leaders, healthcare professionals, and researchers in oncology.
Conduct all interactions in a factual, objective, non-promotional manner, ensuring compliance with company policies and regulatory requirements.
Demonstrate comprehensive expertise in genomic technologies, precision oncology, and emerging evidence to advance precision medicine research.
Illumina is a global leader in DNA and multi-omic sequencing, manufacturing research use only and in vitro diagnostic products. The company employs thousands worldwide and fosters an inclusive culture of openness, collaboration, and belonging, empowering employees to contribute to health equity.
Serve as primary point-of-contact liaison with clients and oversee all aspects of clinical trials.
Manage study budgets, project timelines, risk, and cross-functional teams to ensure quality and compliance.
Drive bid defense preparation, client presentations, and continuous process improvement across assigned portfolios.
Precision for Medicine supports clinical research and development for biopharmaceutical and life science companies. It is a global, collaborative organization that emphasizes quality, innovation, and professional growth.
Execute 12-18 MD-level engagements per quarter across defined geography, with at least 50% in top strategic community accounts.
Serve as primary MD triage for escalated area medical inquiries, ensuring 90% acknowledgment within 48 hours and 100% closed-loop documentation.
Host or present at least 12 regional educational programs per quarter and lead at least one educational initiative per cycle.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team is made up of highly dedicated professionals from world-class institutions, who care deeply about the work and each other.
Lead full service clinical projects in Oncology, ensuring timelines, budget, and quality.
Serve as primary client liaison and coordinate cross-functional teams across all study stages.
Manage all aspects of clinical trials, including proposal strategy, documentation, and reporting.
Precision for Medicine is a CRO enabling precision medicine through novel clinical trial designs, biomarker and data analytics, and a focus on rare diseases and oncology. We are a supportive, collaborative team that values work life balance and development.
Drive product strategy and roadmap for physician-facing RWD applications integrating genomic tests and AI/ML insights.
Own the single- and multi-patient views that bring molecular results and clinical events together.
Partner with cross-functional teams to launch de-identified aggregated research platform for health systems.
Natera is a global leader in cell-free DNA testing for oncology, women's health, and organ health. The company employs a team of highly dedicated professionals from world-class institutions who care deeply about their work and each other.
Serve as primary medical and scientific expert for clinical trial protocols and Expanded Access Programs.
Monitor trials to ensure participant safety, data accuracy, and protocol compliance.
Lead protocol development, investigator training, and cross-functional collaboration.
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, expanded access programs, and market access solutions. With 15+ years of experience across 150+ countries, they offer operational scale and a personalised culture.
Advance the medical strategy within the assigned territory through fair-balanced, evidence-based scientific exchange and credible partnership with the healthcare community.
Deliver high-quality scientific and clinical presentations on disease states and Iovance products to internal and external audiences, tailoring content to audience needs.
Build and sustain relationships with external experts, collect field medical insights, and support clinical trial site identification and execution.
Iovance Biotherapeutics is a global leader in developing tumor infiltrating lymphocyte (TIL) cell therapies for solid tumors. It is an end-to-end cell therapy company with centralized U.S.-based manufacturing, serving thousands of cancer patients worldwide each year.
Conduct high-volume outreach to oncologists, PIs, and research coordinators regarding trial-eligible patients and facilitate referral workflows.
Perform rigorous clinical reviews of patient molecular data against trial inclusion/exclusion criteria using AI-enabled matching platforms.
Provide empathetic education to patients about clinical trial opportunities and maintain meticulous documentation of all activities.
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women's health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply for the work and each other.
Manage all clinical aspects of assigned studies across multiple countries, ensuring timeline adherence and quality.
Lead CRAs and support site selection, start-up, enrolment, monitoring, data cleaning, and close-out.
Identify risks to timelines and collaborate with teams to deliver high client satisfaction.
Precision for Medicine is a precision medicine CRO combining novel trial designs, operational experts, and biomarker analytics with a focus on oncology and rare diseases. It encourages high-energy professionals who thrive in dynamic environments.
Supports clinical trial design, protocol development, and data interpretation to ensure high-quality data generation.
Provides medical expertise in therapeutic areas, reviews safety data, and contributes to regulatory documents.
Collaborates cross-functionally with clinical operations, regulatory affairs, and other teams to align clinical activities with development plans.
Oruka Therapeutics is developing novel biologics for chronic skin diseases. As a publicly traded biotechnology company with a startup culture, it focuses on offering patients greater freedom from conditions like plaque psoriasis.
Drive and execute clinical research and real-world evidence across the product portfolio.
Design protocols, statistical analysis plans, and support regulatory activities.
Generate evidence for product development, reimbursement, and scientific dissemination.
Sequel develops next-generation drug-delivery technology, starting with the twiist Automated Insulin Delivery (AID) System for diabetes management. The company fosters a culture of hard work, fun, and genuine support, with a strong focus on employee well-being and comprehensive benefits.
Provide medical direction and scientific leadership for the pancreatic and colorectal cancer programs.
Lead clinical study subteams, design efficient clinical trials, and monitor safety and efficacy data.
Contribute to global regulatory filings, author clinical documents, and present at scientific meetings.
Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for patients with cancer. The company's programs target the RAS/MAPK pathway, and it is driven by an audacious mission to erase cancer.
Provide medical direction and oversight for clinical trials, including safety monitoring and medical data review.
Partner with GCO to build client relationships and support proposals, feasibility, and business development.
Serve as drug development SME, contributing to protocols, training, and medical strategy across studies.
Fortrea is a global contract research organization providing clinical development and trial management services to pharma/biotech. It fosters a collaborative, family-like culture focused on advancing life-saving therapies.
Lead and develop the West Region Oncology Sales team, driving launch excellence for a personalized mRNA cancer therapy.
Build and execute regional account strategies across complex health systems and oncology practices to achieve sales targets.
Foster a high-performance culture through coaching, compliance, and data-driven decision-making.
Moderna is a biotechnology company pioneering messenger RNA medicines and advancing personalized cancer therapies. It is a high-growth, transformational organization recognized for a bold, relentless, curious, and collaborative culture.
Define medical strategy, target patient profiles, and evidence plans for each asset.
Own scientific communications, including core medical narratives, publications, congresses, and medical information.
Lead external scientific engagement with clinicians, payers, and institutions to drive medical impact.
Click Therapeutics develops and commercializes software as prescription medical treatments, known as Digital Therapeutics. It is a rapidly growing pre-IPO company with an inclusive, diverse workforce united in a mission to provide accessible, safe, and effective treatments.
Design realistic healthcare and medical tasks that challenge advanced AI agents.
Analyze clinical records, research findings, and healthcare data to identify inconsistencies and errors.
Develop reference solutions and evaluation criteria for AI-generated medical analyses.
Anyone AI creates high-quality training and evaluation data for frontier AI models. The company offers flexible, remote contract work focused on expert-driven AI evaluation and improvement.
Direct and manage a team of Project Directors and Project Managers in global project delivery.
Provide leadership and oversight for clinical programs and act as primary escalation point for sponsors.
Optimize profitability, manage resources, and ensure compliance with quality standards and regulations.
Precision Medicine Group provides clinical research and project management services for global clinical trials. The company promotes a culture centered on quality, people, clients, and performance.
Lead clinical operations for a 24/7 virtual care platform integrating primary care, behavioral health, and acute care through text and video interactions.
Own clinical policy, regulatory oversight, and partnership clinic launches while collaborating with practice managers to drive operational improvements.
Serve as a clinical expert to internal and external teams, develop best-in-class training, and support high-quality data and tools.
K Health is an AI-powered virtual care engine that partners with leading health systems to modernize primary care through virtual clinics. Founded in 2016, headquartered in New York City, and backed by over $443.5M, the company values diversity and authenticity while building teams as diverse as the patients they serve.
Lead biopharma oncology partnerships, developing new accounts and growing existing relationships.
Execute complex deals including proposals, pricing, contract negotiations, and closing agreements.
Collaborate cross-functionally with R&D, commercial, legal, and finance to deliver excellent partner experiences.
Guardant Health is a precision oncology company using advanced blood and tissue tests, real-world data, and AI to extend cancer-free time. Founded in 2012, it maintains a collaborative culture and is recognized as a top workplace.
Lead complex client implementations, from customer use cases to success metrics and clinical workflows.
Train and educate customers on BioIntelliSense product offerings and value proposition.
Provide ongoing clinical support and post-implementation optimization while coordinating across teams.
BioIntelliSense is a healthcare technology company providing FDA-cleared wearable monitors, like the BioButton, and AI-driven analytics for early detection of patient decline. The company has a remote-first culture with a global team and offices in Colorado and California.