Sr. Manager, Medical Information & Training
zealandpharma · Cambridge, MA, US · United States · On-site
Posted Oct 7, 2026
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Does it excite you to shape how a growing Medical Affairs organization answers scientific questions, builds knowledge, and trains its team, and do you have a PharmD or other doctorate degree 0and a passion for obesity and metabolic health? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.
Your new position
As Sr Manager, Medical Information & Training, you will own two connected areas of impact: serving as our Medical Information Manager, responsible for answering unsolicited HCP and patient inquiries and ensuring scientifically accurate, compliant content, while also serving as our team's Training & Resource Lead, onboarding and upskilling our Medical Affairs team. This is a unique opportunity to build foundational processes and knowledge resources as we scale our US presence, working across obesity, amylin biology, and our petrelintide pipeline.
We offer exciting responsibilities:
Answer unsolicited HCP and patient inquiries with scientifically sound, timely responses
Own (author) and continuously update standard response documents
Ensure scientific accuracy and compliant content through MLR review
Partner with Legal, Regulatory, and Compliance on early asset development inquiries
Track inquiry trends and surface insights upstream to feed the GMA insights engine
Onboard and train the Medical Affairs team using adult learning and assessment best practices.
Partner with global medical affairs scientific communications team
Own and maintain the team's knowledge base across obesity, amylin, and petrelintide
Lead ongoing product and systems training, and serve as a go-to triage resource cross-functionally
Your profile
You are a scientifically rigorous, detail-oriented communicator who thrives at the intersection of medical information and adult learning. You bring structure to ambiguity, build trusted relationships across Compliance, Regulatory, Commercial, and the MSL team, and enjoy translating complex science into clear, actionable resources for others.
PharmD, MD, PhD, or other doctorate level required
Experience in medical information and/or medical communications within pharma or biotech
Experience designing and delivering training programs (adult learning and assessment methodology)
Strong understanding of MLR review processes and compliance requirements in medical communications
Exceptional written and verbal communication skills, with the ability to translate scientific content for varied audiences
Ability to build cross-functional relationships with Compliance, Regulatory, Commercial, and MSLs
Your new team
You will report to Gabe Smolarz, US Medical Affairs, joining our growing US Medical Affairs organization at a pivotal moment as we build out our Boston hub and prepare for the petrelintide launch. Key partners include Compliance, Regulatory, Commercial, and our Medical Science Liaison (MSL) team.
Let's bond and be bold
We have a…