Medical Director, Immunology

EMD Group · Billerica, MA

$175k – $262k/yrPosted Jul 14, 2026

Work Your Magic with us! Start your next chapter and join EMD Serono. 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. Your RoleAs a Medical Director in Immunology, you will play a pivotal role in advancing clinical development programs for immune-mediated diseases — from study design through execution, data interpretation, and regulatory documentation. In this role, you will serve as a key clinical voice within global cross-functional teams, contributing to the scientific rigor and strategic direction of immunology assets that have the potential to address meaningful unmet patient needs. You will provide day-to-day medical oversight for assigned clinical studies, including safety data review, protocol deviation assessment, and interpretation of accumulating efficacy and biomarker data.

Working closely with experienced medical and functional leaders, you will contribute to clinical development planning, support governance discussions with well-reasoned medical analyses, and help shape evidence generation strategies across assigned indications. You will also contribute to regulatory documents and health authority interactions, ensuring all deliverables are scientifically sound, compliant, and inspection-ready. This position offers a clear pathway toward broader program-level medical leadership, with increasing ownership of study strategy and cross-functional decision support as you grow within the organization. What Success Looks LikeThe successful candidate will be scientifically curious, clinically grounded, detail-oriented, and comfortable operating in a global matrix environment.

They should be able to synthesize clinical and safety data, ask practical development questions, communicate clearly, and escalate issues appropriately while learning from senior medical leaders. Success in this role requires balancing strong medical judgment with openness to coaching, collaboration, and increasing responsibility. The ideal candidate will bring credibility with clinical and scientific stakeholders, strong ownership of assigned deliverables, and a clear motivation to grow in pharmaceutical clinical development. Who You AreMinimum Qualifications:<ul style="margin-bottom: 4.0pt; margin-top: 0.0px;"><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Medical degree (MD, DO, or international equivalent) with prior clinical training and hands-on patient-care experience in a relevant medical specialty.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Minimum 3 years of experience in pharmaceutical, biotechnology, academic clinical research, or clinical development; candidates with strong clinical and academic research backgrounds motivated to transition into industry clinical development are also encouraged to apply.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Clinical experience in Rheumatology, Clinical Immunology, immune-mediated inflammatory diseases, Internal Medicine, or a closely related field.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Solid understanding of clinical trial conduct, medical monitoring principles, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, and patient safety expectations.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Demonstrated ability to interpret clinical and safety data, identify medically relevant issues, and communicate findings clearly to cross-functional partners.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Proven ability to deliver assigned milestones and work effectively in a global matrix environment.</li></ul> Preferred Qualifications:<ul style="margin-bottom: 4.0pt; margin-top: 0.0px;"><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Board eligibility, board certification, fellowship training, or equivalent specialist qualification in Rheumatology, Clinical Immunology, Internal Medicine with immunology focus, Dermatology, Gastroenterology, Nephrology, or another relevant immune-mediated disease area.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Experience supporting clinical trial design, execution, data review, medical monitoring, or study-level decision-making.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Familiarity with global clinical trial conduct, regulatory submissions, and health authority interactions.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Experience preparing or reviewing clinical documents such as protocols, informed consent forms, investigator brochures, clinical study reports, or scientific communications.</li><li style="margin: 0.0in 0.0in 4.0pt 0.0px; line-height: normal; font-size: 12.0pt; font-family: Aptos, sans-serif;">Strong knowledge of drug development and clinical trial methodology in immune-mediated inflammatory diseases, rheumatology, or related therapeutic areas. </li></ul> Location: Billerica, MA, USA; Onsite (3x week) Travel: <20%; International and Domestic Pay range for this position: $200,800.00 - $301,300.00 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. For more information click <a href="https://careers.emdgroup.com/us/en/benefits">here</a>. What we offer: 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! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Originally posted by EMD Group. View original posting

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