Clinical Research Scientist (all genders)

at  Merck Group

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.

The Clinical Research Scientist (CRS) represents and may lead clinical activities on the assigned oncology clinical study(ies) and/or project(s) within global clinical development oncology. You interact with the multi-disciplinary, matrix, global teams ensuring that scientific, clinical and other topics are appropriately considered with respect to highly complex data findings and escalated to Clinical Lead(s) as appropriate.

As an individual contributor, you will

• have significant impact on the creation, maintenance, and execution of the clinical study protocol or the clinical development plan in the development of the company’s oncology portfolio
• Collaborate with Medical Directors / Clinical Leads in creation of proposed concept sheets for clinical studies
• Communicate and train clinical development team members, as well as other teams (i.e clinical operations, etc) in new scientific directions within the oncology program(s)
• Drive creation and annual update of relevant study documents (protocol, IB, DSUR, etc.)
• Collaborate with Medical Directors / Clinical Leads to ensure medical and scientific data surveillance of ongoing clinical studies.