EPM Scientific

We are excited to announce that EPM Scientific will be attending MEDICA - Leading International Trade Fair in Düsseldorf on Tuesday 12th November! One of the largest medical B2B trade fairs in the world, the event will share some of the latest innovative products and services in the evolving healthcare sector. Representing EPM Scientific and keen to connect with new and familiar faces are: • Beth Frost- Associate Vice President • Conor O'Sullivan- Consultant If you can’t attend but would like to discuss how EPM Scientific can support your hiring needs, please request a call back here: https://hubs.la/Q02XfWkj0

New Role: VP Regulatory Affairs Apply: https://hubs.la/Q02X8hYg0 Location: San Francisco, CA Salary: US$330,000 - US$365,000 per annum A rapidly growing biotech in CA is seeking a highly experienced regulatory affairs professional to join their team. This company has seen massive growth over the past decade and just had an incredible data readout. They are excited to welcome on a new member of the leadership team to oversee the RA functions and lead the NDA process through launch. Requirements: • 15+ years of experience in regulatory affairs in biopharma/biotech/pharma • Advanced degree preferred (MD, PhD, PharmD, MS) • Previous NDA and small molecule experience is desired • Has experience managing multiple assets in a product pipeline 💡 Learn more about this #opportunity by applying.

Talent strategy plays a critical role in driving growth. If there’s a role to be filled at your life sciences company, you might be wondering whether a permanent or contract hire is the best fit. In this article, EPM Scientific takes a closer look at the different advantages of hiring permanent and contract employees, and how they can uniquely contribute to the success of your business. ➡️Read more here: https://hubs.la/Q02RDnxb0 #TalentStrategy #LifeSciencesIndustry #WorkforcePlanning

We are excited to announce that Samm Zombolo, Senior Vice President at EPM Scientific, has been appointed as London Chapter Board Member - Volunteer & Engagement at the Healthcare Businesswomen’s Association. The Healthcare Businesswomen’s Association (HBA) is a global professional association committed to furthering the advancement and impact of women in the business of healthcare. As a London Chapter Board Member and Senior Vice President at EPM Scientific, Samm Zombolo will be able to provide support and opportunities to members within the life sciences industry. If you would like to get in touch with us about your hiring needs or the next step in your career, please reach out to us: https://hubs.la/Q02W9c5-0

New Role: Director of Biopharma Technical Services Apply: https://hubs.la/Q02VZb4s0 Location: Boston, MA Salary: US$150,000 - US$200,000 per year This Director of Biopharma Technical Services position will lead the technical support team of an organization in the genetic and genomic clinical testing industry, ensuring the successful implementation, maintenance, and growth of pharmaceutical and biotech partnerships. The role requires a strategic thinker with strong leadership skills and a deep understanding of the pharmaceutical/biotech industry, genomics, and proteomics. Requirements: • PhD in life sciences required • Experience in CRO/pharma required • Translational/biomarker experience preferred 💡 Learn more about this #opportunity by applying.

Are you staying up-to-date with talent and compensation trends in the commercial sector? Download EPM Scientific’s Global Commercial Market Update & Salary Guide to access exclusive insights and salary benchmarks, helping you make informed hiring decisions or confidently plan your career in sales, marketing, or operations within the life sciences industry. ➡️Get your copy here: https://hubs.la/Q02R-0-S0

Earlier this month, EPM Scientific was grateful to have partnered with DFW Healthcare Businesswomen's Association to sponsor their latest panel and networking event, "The Commercial Edge: Mastering Business, Recruitment, and Talent Retention" right here in our Dallas office. Special thanks to Carrie Graham, Chase Wasson, Lauren D'Angelo, and Perry Monaco for serving as our panelists, to our very own Kristiaan Rawlings for being an excellent moderator, and to all that were able to attend. To learn how EPM Scientific can support your business' commercial hiring and retention goals, request a call back today: https://hubs.la/Q02V3_Pf0

Join us this Thursday, October 24th in our Berlin office for an insightful networking event and panel discussion about 'Exploring the Potential of AI in Clinical Trials, Future Planning, and Challenges'. We are excited to announce the panellists sharing their expert insights: • David Higgins, CTO Consultant • Markus A. Dahlem, VP Science, Click Tx • Adjmal Sarwary, Medtech & AI Consultant • Karym El Sayed, Head of eHealth & Medical Software, Bayer If you are interested in attending the event, or would like more information, please contact: hashan.alwis@epmscientific.com. If you can't attend, but would like to speak to our team of experts about your hiring needs and opportunities, request a call back today: https://hubs.la/Q02V4DVq0

🔎Looking for your next challenge in the life sciences industry? At EPM Scientific, we specialize in connecting talented professionals with career-defining global opportunities in life sciences. Whether you're ready to step into a leadership position or explore a new area of expertise, we have exclusive roles waiting for you. ➡️Browse our latest roles: https://hubs.la/Q02RCqrT0

New Role: Vice President Regulatory Affairs Apply: https://hubs.la/Q02Tdbhv0 Location: San Francisco, CA Salary: US$330,000 - US$365,000 per annum A rapidly growing biotech in CA is seeking a highly experienced Regulatory Affairs professional to join the team as the VP Regulatory Affairs. This company has seen massive growth over the past decade and just had an incredible data readout. They are excited to welcome a new member of the leadership team to oversee the RA functions and lead the NDA process though launch. Responsibilities: - Provide regulatory leadership through the regulatory strategy of product development and approval - Provide knowledge of global quality/regulatory guidelines and ensure requirements are met across programs - Partner with internal senior leadership to collaborate on cross-functional projects and provide global regulatory plans to align with company objectives - Have ownership of relevant regulatory submission deliverables - Provide leadership and oversight of all critical global regulatory submissions (pre-IND through post-marketing) to FDA and RoW notified bodies - Represent the Regulatory department in senior management discussions and present strategies, risk assessments, and recommendations - Provide hands on leadership for the Regulatory department Requirements: - 15+ years of experience in Regulatory Affairs in biopharma/biotech/pharma - Advanced degree preferred (MD, PhD, PharmD, MS) - Previous NDA and small molecule experience is desired 💡 Learn more about this #opportunity by applying.