Are you motivated to participate in a dynamic, multi-tasking environment? Do you want to join a company that invests in its employees? Are you seeking a position where you can use your skills while continuing to be challenged and learn? Then we encourage you to dive deeper into this opportunity.
We believe in career development and empowering our employees. Not only do we provide career coaches internally, but we offer many training opportunities to expand your knowledge base! We have highly competitive benefits with a variety HMO and PPO options. We have company 401k match along with an Employee Stock Purchase Program. We have tuition reimbursement, leadership development, and even start employees off with 16 days of paid time off plus holidays. We offer wellness courses and have highly engaged employee resource groups. Come join the Neo team and be part of our amazing World Class Culture!
NeoGenomics is looking for a Senior Advisor, Medical Affairs wants to continue to learn in order to allow our company to grow. This is a remote position with a Monday – Friday day shift.
Now that you know what we're looking for in talent, let us tell you why you'd want to work at NeoGenomics:
As an employer, we promise to provide you with a purpose driven mission in which you have the opportunity to save lives by improving patient care through the exceptional work you perform. Together, we will become the world's leading cancer reference laboratory.
Position Summary:
As a Senior Advisor, Medical Affairs you will be a member of the Clinical Programs team at NeoGenomics, assigned to collaborate and engage internally with NeoGenomics research and development, clinical testing, pharma, and product/marketing, and externally with Key Opinion Leaders (KOLs)/Scientific Advisors, and clinical investigators to gain clinical insights and support clinical trial efforts. This role is responsible for clinical subject matter expertise of NeoGenomics assays to support further enhancement of NeoGenomics clinical development.
Responsibilities:
- Collaborate and engage with various internal departments including R&D, product, pharma, clinical sales, marketing, legal, regulatory, and managed care
- Analyze and monitor competitor data/clinical trials (relevant to NeoGenomics) and gather KOL insights
- Use this knowledge to guide clinical strategy and inform clinical, R&D, and commercial teams.
- Facilitate knowledge and education of relevant medical and scientific content and NeoGenomics products to internal team departments
- Serve as advisor for advanced technical questions about NeoGenomics assays
- Participate in medical updates, scientific presentations, journal clubs, teleconferences and meetings as a primary clinical resource
- Provide scientific and clinical support about NeoGenomics assays to Market Access/Reimbursement teams • Support MolDX dossiers and similar submissions to regulatory/reimbursement groups
- Leverage clinical/scientific data to support Product/Marketing needs, including authorship of manuscripts and whitepapers
- Collaborate with the field Medical Affairs team to support, educate and respond to unsolicited questions from the medical community
Experience, Education and Qualifications:
- Master’s Degree or Ph.D in a life science, health service, or related field, or Medical Degree.10+ years of hands-on experience in software development and architecture, ideally with a focus on healthcare or laboratory systems.
- 10+ years of experience or research in genetics, molecular biology, oncology, or related field
- 5+ years of medical affairs or clinical development experience in the medical device, biotech, or pharmaceutical industry; Medical affairs field experience strongly preferred
- Scientific and technical experience in the field of oncology
- Demonstrated comprehensive understanding of principles for study design and data analysis, and the ability to critically evaluate study results
- Experience in interfacing with key opinion leaders including physicians
- Ability to partner and maintain relationships within the medical community
- Solid understanding of medical treatment / patient management and clinical workflows
- Computer literacy (including relevant software, such as Excel, Word, PowerPoint, Adobe)
- Proven ability to work independently as well as in cross-functional networks
- Excellent written and verbal presentation skills with the ability to generate high-impact slides and to tailor technical delivery based upon the specific audience
- Ability to travel up to 10% of the time
Equal employment opportunity, including veterans and individuals with disabilities.
PI275400211
