Principal, Medical Affairs Innovation
ExternalPrepare for this interview
EliteAI-generated questions, company research, and talking points tailored to this role
About the role
The Principal, Medical Affairs Innovation will be responsible for supporting innovation projects in the Specimen Management business unit. You will be a member of a dedicated cross-functional innovation team responsible for developing and delivering upon the innovation strategy to drive growth for the business unit. You will identify, evaluate, and advance projects through the innovation funnel and lead clinical assessment and strategy for innovation projects. Additionally, you will generate, synthesize, and communicate clinical evidence to support product development and regulatory submissions. The ideal candidate will utilize exceptional verbal and written communication skills, including the ability to author peer-reviewed scientific papers, develop technical documentation, and deliver impactful presentations. Experience demonstrating a capacity to exercise independent judgment and discretion within broad policy frameworks, leveraging analytical problem-solving to address complex challenges is necessary. Having proven effectiveness in managing complex projects involving ambiguity, rapid change, and cross-functional collaboration will be key! Job Responsibilities: You will work with R&D, marketing, HEOR, and regulatory team members to evaluate different innovation ideas and support these projects through the innovation pipeline. You will interact with external stakeholders, including healthcare providers, academic & industry experts, payers, regulatory bodies, and policymakers to identify unmet needs relating to specimen management and collection You will draft clinical and laboratory workflows, perform literature review, guide market landscape assessment, and gather customer feedback to provide a detailed clinical assessment of the innovation project. You will be responsible for outlining the medical strategy and leading evidence generation initiatives, including study design, protocol development, and execution. Oversee publication strategies and prepare reports, abstracts, journal manuscripts, and presents findings at external scientific meetings or internal BD forums. Review and interpret medical and scientific data, study results, and technical literature. Monitors trends in specimen management and related technologies. Design studies and lead scientific investigations, feasibility assessments, and due‑diligence evaluations related to new technologies and products. Collaborate with and relay findings to the new product development team Attend medical and healthcare conferences, workshops, and meetings to stay abreast of both medical practice, medical guidance and healthcare trends and best practices Minimum Required: Bachelor of Science (BS) in a health-related field, such as Biochemistry, Chemistry, Microbiology, Molecular Biology, or similar disciplines 7+ years of clinical laboratory experience. Experience managing multiple priorities, scheduling tasks effectively, and delivering results within tight timelines to meet evolving business needs. Experience comprehending, interpreting, and clearly communicating complex clinical and scientific information in a concise and accessible manner. Experience utilizing consistent attention to detail, ensuring accuracy, completeness, and compliance in all work products and deliverables. Has advanced knowledge of scientific methodologies and their application in clinical laboratory medicine. Solid understanding of clinical studies, including study design, execution, data interpretation, and analysis. Preferred Knowledge and Skills: Master of Science (MS) degree in a health-related field, such as Biochemistry, Chemistry, Microbiology, Molecular Biology, or similar disciplines + 3 years minimum of clinical laboratory or research experience PhD in a relevant field (such as Clinical Chemistry). Experience in a medical device, IVD, or pharmaceutical company. ASCP MLS certification (or equivalent), advanced training, or board certification in clinical chemistry, microbiology, molecular biology, or other specialized clinical laboratory disciplines. Pay Transparency Statement: At BD, we are committed to supporting our associates' well-being, development, and success through a performance-based culture. For this position, BD offers a competitive compensation package along with the following benefits specific to this role: - Annual Bonus - Potential Discretionary LTI Bonus Health and Well-being Benefits - Medical coverage - Health Savings Accounts - Flexible Spending Accounts - De
Benefits
Additional Information
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. Job Description
Your Match
How well this role fits your profile.
Company Intel
What employees say
Worked at Becton Dickinson? Share your experience