Senior Clinical Scientist

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 Senior Clinical Scientist (CRS), you will serve as a subject matter expert and strategic partner to the Medical Lead, providing scientific, clinical, and operational input across early and late-stage clinical development programs.
In this role, you will:
Contribute to data interpretation, study designs, regulatory and study documents, and publication efforts
Provide scientific input into pipeline programs
Conduct Medical Monitoring and Medical Data Review activities in close collaboration with the Medical Lead, including oversight of Medical Monitoring activities performed by contracted vendors
Engage and collaborate with a multi-disciplinary, global team, ensuring that scientific, clinical, and other relevant topics are appropriately considered in the context of highly complex data findings
Who You Are
You are an experienced clinical research professional with a strong scientific background and a passion for advancing innovative therapies.
Minimum Qualifications:
Master's Degree
Minimum of 3 years of experience in product and clinical development, with at least 5 years in a comparable role within the pharmaceutical, biopharmaceutical, or healthcare industry
Preferred Qualifications:
Advanced degree in life sciences (e.g., PharmD, PhD, or MPH) and postdoctoral experience preferred
Proven track record of successfully leading or making significant contributions to clinical trials, with Phase III experience strongly preferred
Educational and/or professional background in immunology is strongly desirable, with the ability to rapidly develop a working scientific knowledge across different therapeutic areas
Skills & Competencies:
Ability to work both independently and collaboratively on tasks and projects of increasing complexity, with a commitment to scientific rigor
Solid knowledge of regulatory requirements, including ICH-GCP guidelines
Strong aptitude for interpreting and integrating complex data sets, including clinical safety and efficacy data, pharmacokinetics, biomarker data, and next-generation sequencing data
High level of medical and clinical knowledge, with hands-on experience in clinical development and operations, including the ability to monitor laboratory and other clinical trial data
Excellent communication and presentation skills, with the ability to contribute to abstracts and publications and to adapt messaging effectively for a variety of audiences
Location: Billerica, MA (3 days per week – Tuesday, Wednesday, Thursday)
Travel