At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented
Job Description The Associate Director, Pharmacovigilance Scientist plays a critical role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. This individual also serves as a subject matter expert
Job Title: Global Development Scientist, Associate Director Waltham, MA / Boston, MA Introduction to role: Are you ready to shape the clinical strategy that accelerates transformative immunotherapy and cell therapy for blood cancers from concept to
Job Title: Global Development Scientist, Director Waltham, MA / Boston, MA Introduction to role: Are you ready to steer global hematology trials that turn bold science into life-changing medicines? As Global Development Scientist, Director, you will
We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your
This job is with Biogen, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. The Manager, Informed Consent Management Oversight
Manager, Commercial Energy Location: Remote MA Ready to make a difference? We are currently seeking a Manager, Commercial Energy to join our Northeast Energy Efficiency team to provide critical program support and technical services for Massachusetts
Sr. Medical Director/Medical Director, Global Safety Officer (GSO) The Sr. Medical Director/Medical Director, Global Safety Officer (GSO) will work closely with the DSPV leadership team and will provide strategic safety oversight for the assigned investigational and/or
Role Overview And Key Functions The Medical Director, Pharmacovigilance (PV) will provide broad support of activities requiring medical safety input for assigned products, pre- and post-approval. He/she will support and/or lead periodic safety signaling reviews and