Research Biomedical Coordinator

We are a team of dedicated professionals driven by a shared mission to serve patients living with serious illnesses.

Our organization has been pioneering the world of biotech since 1980, focusing on four therapeutic areas: Oncology, Inflammation, General Medicine, and Rare Disease. As a member of our team, you will contribute to making a lasting impact on the lives of patients by researching, manufacturing, and delivering innovative medicines.

We have an award-winning culture that is collaborative, innovative, and science-based. If you thrive in challenging environments and are passionate about growth opportunities, you will excel as part of our team.

• You will represent the local functional management team within Global Study Operations Site Management (GSO-SM) and ensure the overall quality of work performed by SM-FSP staff supporting clinical trials.
• Lead and manage contract responsibilities for both Amgen-sponsored and investigator-sponsored clinical trials, including managing contracts, resources, capacity planning, and performance to ensure timely and compliant trial delivery.

• You must have a Doctorate degree or a Master's degree with 2 years of work experience in life sciences or a medically related field, including biopharmaceutical clinical research.
• Prior experience in clinical research, including clinical site management, obtained working on clinical trials in a biotech, pharmaceutical or CRO company, or other relevant clinical setting is highly valued.

We offer a competitive benefits package and a collaborative culture that supports your professional and personal growth and well-being.

In addition to the base salary, we offer comprehensive Total Rewards Plans aligned with local industry standards.

We foster an inclusive environment of diverse, ethical, committed, and highly accomplished people who respect each other and live our values.