Medical Director in Global Clinical Development Oncology

EMD Group · Billerica, MA

$175k – $262k/yr

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 Role:As a Medical Director in Global Clinical Development Oncology, you will provide clinical and scientific leadership for development programs in oncology, ideally with experience in targeted therapies, antibody-drug conjugates (ADCs), and/or immuno-oncology. Next to experience with drug development for solid tumors, experience with hematology/hematologic oncology is viewed favorably. In this role, you will independently drive day-to-day clinical development activities while contributing to high-quality execution of the overall clinical strategy in a global matrix environment.Key Accountabilities:<ul style="margin-bottom: 0in; margin-top: 0px;"><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Lead assigned clinical studies and contribute to broader program strategy across the development continuum, from Phase 1 through Phase III, including support for registration-enabling activities, regulatory submissions, and Health Authority interactions.</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Integrate clinical, translational, biomarker, and emerging data to support indication strategy, patient selection, dose strategy, and key development decisions. </li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Operate as a core member of cross-functional teams and the Global Project Team, partnering closely with Program Leadership and Management, Translational Medicine, Biostatistics, Clinical Pharmacology, Regulatory Affairs, Clinical Operations, Safety, and Medical Writing. </li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Support study design, dose strategy, patient selection, and indication prioritization</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Integrate clinical, translational, and biomarker data into development decisions</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Provide medical monitoring and clinical oversight for assigned studies</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Review and interpret safety and efficacy data to support study decisions</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Author and contribute to key clinical and regulatory documents, including protocols, investigator brochures, clinical study reports, briefing books, submission documents, and dossiers</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Contribute to registration-enabling activities and regulatory submissions</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Support interactions with Health Authorities and internal governance bodies</li><li style="line-height: normal; margin: 0in 0in 0in 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Drive execution of deliverables across global teams and timelines</li><li style="line-height: normal; margin: 0in 0in 8pt 0px; font-size: 12pt; font-family: Aptos, sans-serif;">Contribute to a high-performing, collaborative matrix environment.</li></ul> Who You AreMinimum Qualifications:<ul style="margin-top: 0in; margin-bottom: 0in;" type="disc"><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">MD with expertise in clinical drug development</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Required expertise in Oncology</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Minimum 3 years of industry experience in clinical R&D within pharma/biotech</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience supporting or leading clinical studies across Phase 1 through Phase III</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience contributing to clinical development strategy, regulatory submissions, and registration-enabling activities</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Familiarity with clinical dossiers, regulatory documentation, and Health Authority interactions</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Demonstrated ability to integrate translational and biomarker data into clinical development decisions</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience working in cross-functional, matrixed, and international teams</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Familiarity with ICH-GCP, FDA and/or EMA expectations, and clinical trial regulations</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Strong written and verbal communication skills in English</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to work independently, manage multiple priorities, and collaborate across time zones in an office-based environment.</li></ul> Preferred Qualifications:<ul style="margin-top: 0in; margin-bottom: 0in;" type="disc"><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience in targeted therapies, ADCs, immuno-oncology, and/or hematology/hematologic oncology</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience across early and late clinical development</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience contributing to study designs that support potential registration pathways</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Experience with precision medicine, and/or biomarker-driven development</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Strong project leadership skills with a track record of driving timelines and decision points</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Board certification in Medical Oncology/Hematology or relevant subspecialty.</li></ul> Key Competencies<ul style="margin-top: 0in; margin-bottom: 0in;" type="disc"><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Strong clinical judgment in oncology</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Scientific and analytical rigor</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Ability to translate complex clinical, translational, and biomarker findings into development strategy</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Effective cross-functional collaboration; team player mentality</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Clear and concise communication</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Ownership, accountability, and execution focus</li><li style="margin-bottom: 0in; margin-top: 0in; line-height: normal; margin-right: 0in; font-size: 12pt; font-family: Aptos, sans-serif;">Comfort working in a fast-paced, global matrix organization</li></ul> Location: Billerica, MA, USA; Onsite (Hybrid) Travel: <20%; International and Domestic Pay range for this position: $174,600.00 - $262,000.00 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

← Browse all companies

BioCareerAI is an independent job platform and is not affiliated with or endorsed by EMD Group.