MDWerks Inc.

Compensation

Full Description

Job Description: • oversee the development and dissemination of symposia, videos, podcasts and other medical education content to support our clinical research initiatives • Deliver high-quality, impactful scientific content that support both internal stakeholders (e.g., Field Medical) and external stakeholders (e.g., healthcare professionals). • Assist with development, review and/or maintenance of product and disease-related slide kits, symposia, digital education • Leverage digital (SERMO, podcasts, videos), omnichannel tools, and AI-driven solutions to innovate and enhance Medical Communication strategies • Contribute to medical congress activities, as needed, including support for booth content, scientific content and session coverage; create post-congress summary materials • Own the development, pull-through and execution of the Scientific Narrative and Scientific Communication Platform (SCP). • Participate in the creation and execution of scientific content plan for the fiscal year, including alignment with the Medical Plan • Develop program specific scientific materials such as mechanism of disease or action graphics, data summary decks, and templates for company wide use. • Manage external vendors and agencies to deliver high-quality live and virtual medical education programs. • Monitor and assess the effectiveness of medical education initiatives and provide feedback to cross functional teams for continuous improvement. • Align with cross-functional teams to develop a dynamic and evolving Independent Medical Education program. Requirements: • Must have an advanced medical degree (MD, DO, or equivalent), PharmD or PhD. • 3+ years of medical affairs experience in the Pharmaceutical/Biotechnology industry • Experience in hypertension, sleep apnea, chronic kidney disease, launch experience preferred • Experience in budget and vendor management • Proven success in a fast-paced, entrepreneurial, smaller company environment is highly desired. • Proven experience in working collaboratively and cross functionally across field medical teams, corporate affairs, clinical development, commercial, sales, market access and other key functions and demonstrated ability to inform and shape company/product strategy. • Demonstrated understanding of laws, regulations, standards, and guidance governing the conduct of publications. • Proven experience collaborating with cross-functional, international teams. • Strong understanding of compliance and regulatory frameworks governing scientific exchange. • Strong understanding of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GPP, ICH, PhRMA Code). Benefits: • standard Company benefits including medical, dental, vision, time off and 401K • participating in Mineralys incentive plans are contingent on achievement of personal and company performance