Clinical Science Team Lead / all genders / Part- Fulltime

Work Your Magic with us!  

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.

Your Role: 

The  Clinical Science Lead, will supervise and manage  a team of Clinical Research Scientists (CRS) within the Global Clinical Development Oncology unit. The incumbent will ensure the functional excellence and standardization of the CRS group's contributions to the clinical projects and programs from phase 1 to 3. He/She will manage the CRS resources efficiently and proactively for the various clinical projects of the DU Oncolog and will define and conduct the training for the CRS group in alignment. Responsibilites: Supervise and manage a team of Clinical Research Scientists (CRS) within the Global Clinical Development unit. You ensure functional excellence across the group of CRS by defining an aligned training and development path for his/her team. You are responsible of the standardization of the contributions of the CRS to the preparation, conduction and interpretation of clinical studies. You providing guidance and supervision to the CRS to ensure working in close partnership with CROs and other vendors as appropriate. You ensure that clinical programs and projects are efficiently staffed with CRS resources, identifying proactively resource gaps and find proactively solutions to cover those. You are responsible that new clinical programs are adequately staffed to provide Medical Review according to HOM and being responsible to request FSP resources from CROs if applicable.You act as a BPO for certain processes in which the CRS role is prominent. 

Who you are: 

• Advanced degree in life sciences (e.g., PharmD, PhD, MS, MPH) or MD.

• At least 10 years’ experience in pharmaceutical industry & clinical development

• At least 5 years’ experience as CRS  or a proven equivalent position

• Track record of leading people in teams (direct or cross-functional)

• Strong communication skills - verbal, written and listening,

• Educational and/or work experience in the respective therapeutic area in Oncology  is strongly desirable.

• Experience interacting with development operations (clinical operations, regulatory, QA) and clinical investigators.

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!