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EMD Serono, Inc. is seeking an Associate Director, Preclinical Pharmacology to lead in vivo pharmacology for Fertility assets. The role involves designing and interpreting studies, shaping translational strategies, and contributing to IND-enabling packages.
You will collaborate with Immunology, Neuroscience, and DMPK teams, manage CROs, and drive KPI-driven program milestones in a hybrid work setting in the U.S.
Work Your Magic with us! Start your next chapter and join EMD Seronto.
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
The Associate Director, Preclinical Pharmacology (reporting to the Head of Preclinical Pharmacology, Research Unit Neuroscience & Immunology) serves as the scientific and operational lead for in vivo pharmacology across the Fertility asset portfolio, with cross-disciplinary contributions to Immunology & Inflammation (I&I) and Neuroscience programs. Working within a cross functional project team, you will lead multiple, high-priority fertility programs, accountable for designing, executing, and interpreting in vitro and in vivo studies that drive candidate selection, dose regimen design, and translational strategy, ultimately contributing to IND-enabling packages and regulatory submissions.
Hybrid – 3x/week onsite in Billerica, MA required.
$126,900 – 215,400
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job‑related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites.
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!