Work Your Magic with us! Start your next chapter and join MilliporeSigma.
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.
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 lead the development and execution of clinical strategies for oncology projects. You will provide strategic and medical leadership across cross-functional teams, guiding clinical studies from early to late-stage development and collaborating with the Global Project Team (GPT).
Key Accountabilities:
• Oversee clinical study projects from Phase 1 to Phase 3 within the Clinical Team.
• Serve as a clinical expert in dedicated programs within the GPT.
• Design clinical development strategies for early and late phases.
• Potentially supervise Clinical Research Scientists (CRS).
• Offer medical expertise for business development, discovery, stratified medicine, and regulatory affairs.
• Develop clinical plans, study concept sheets, and protocols in collaboration with team members.
• Ensure high-quality clinical documents, including protocols, reports, and Investigator Brochures.
• Review and approve clinical documents and analyze study data.
• Provide medical supervision for assigned projects/programs.
Who You Are
Minimum Requirements:
• MD with expertise in clinical drug development.
• Minimum 3 years of experience in clinical R&D within the pharmaceutical or biotech industry.
• Experience interacting with Health Authorities in Europe, the US, and possibly Japan/China.
• Ability to work in a matrix environment and within international cross-functional teams.
• Strong team player with excellent communication skills in English.
Preferred Requirements:
• Experience in oncogenic signaling clinical development.
• Familiarity with R&D interface partners (e.g., Regulatory Affairs, Clinical Pharmacology).
• Project management skills.
• Understanding of R&D and non-R&D partner needs.
• Strong analytical skills, strategic orientation, and initiative.
• Ability to multitask and adapt in a dynamic environment.
Pay Range for this position: $230,000 to $309,000
Our ranges are derived from several sources, and largely reliant on relevant industry market data. Should we decide to make an offer, we will consider several factors, including but not limited to your location, skills, experience, career level, and other job-related factors. This role may offer the following benefits: medical, vision, and dental insurance; life insurance; disability insurance; a 401(k) matching program; paid time off; and paid holidays; among other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including, but not limited to, cash bonuses.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html