Zealand Pharma
Sr. Manager, Medical Information & Training
Cambridge
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Lead / management
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 1 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
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 and 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.
LOCATION: remote/hybrid (Northeast USA)
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 Global Medical Affairs, 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.
- 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 GMA, Compliance, Regulatory, Commercial, and the MSL team, and enjoy translating complex science into clear, actionable resources for others.
- PharmD 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
- Excellent 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 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 US Medical Affairs (field medical MSLs and home office team) ,Global Medical Affairs, Compliance, Regulatory, and Commercial.
Let's bond and be bold
We have a unique culture, characterized by excellent teamwork and strong engagement across the organization. And we want you to help us strengthen this culture.
Making bonds is at the core of everything we do. From discovering and developing the best new peptide drugs for patients, to engaging with our partners or connecting with each other. We bond through curiosity and playfulness as a team, allowing ourselves to challenge common thinking and drive future innovation. Join us and let's bond and be bold.
Interested in bonding with us? The applications will be reviewed as they come in. While a cover letter is not required, please include a few sentences in your CV explaining your motivation for applying.
We are committed to an inclusive recruitment process and welcome applications from all job applicants.
About Zealand Pharma A/S
Zealand Pharma A/S (Nasdaq: ZEAL) is a biotechnology company focused on advancing medicines for obesity and metabolic health. Combining more than 25 years of peptide R&D expertise with a proprietary data platform that leverages advanced data-driven and AI/ML approaches, Zealand Pharma aims to lead a new era in obesity and metabolic health. To date, more than ten Zealand Pharma-invented drug candidates have entered clinical development, of which two products have reached the market and three candidates are in late-stage development. The Company has collaborations with global pharmaceutical and biotechnology partners for research, development, and commercialization. Founded in 1998, Zealand Pharma is headquartered in Copenhagen, Denmark, with a U.S. presence in Cambridge, Massachusetts. Learn more at www.zealandpharma.com .
Similar jobs
- Assistant Nurse ManagerVeterans Health Administration · Atlanta, Georgia, United StatesFirst seen today
- Supervisory Financial Management Specialist - Facility Revenue ManagerVeterans Health Administration · Brockton, Massachusetts, United StatesFirst seen today
- Program ManagerInternal Revenue Service · Anchorage, Alaska, United StatesFirst seen today
- Supervisory Air Traffic Control Specialist, Assistant General ManagerFederal Aviation Administration · Minneapolis, Minnesota, United StatesFirst seen today
- Supervisory Air Traffic Control Specialist, (MSS-3, Level 10), Operations ManagerFederal Aviation Administration · Seatac, Washington, United StatesFirst seen today
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job