Explore 21 Remote Biopharmaceutical Jobs
The Associate Director, Field Reimbursement will enhance patient access to treatments for Spinal Muscular Atrophy through strategic account management and education.
The Rx Onboarding and Care Coordinator ensures personalized care and support for patients with spinal muscular atrophy throughout their treatment journey.
A.B.S.C
Advanced Bio-Logic Solutions Corp
The Senior Associate Regulatory Affairs (CMC) role involves supporting regulatory submissions and managing projects in a remote setting.
The Upstream Manufacturing Associate will optimize bioreactor performance and improve manufacturing techniques in a biopharmaceutical setting.
J.E.B
Just - Evotec Biologics
The Senior Vice President of Business Development will lead strategic partnerships and business transactions to drive growth for Just-Evotec Biologics.
The Hematology Clinical Account Manager is responsible for driving sales and promoting Sobi products within the Omaha territory.
The Manager, GCP Quality Assurance will oversee compliance and quality assurance for clinical trials at Madrigal.
I.C
IMVT Corporation
Immunovant is seeking a Senior Director for Clinical Quality Assurance to lead quality efforts and ensure compliance with global regulations.
The Clinical Research Medical Director will lead obesity-related studies and integrate scientific insights into the development of innovative treatments.
A.P
Acadia Pharmaceuticals
Join Acadia Pharmaceuticals as a Regional Marketing Liaison focusing on rare diseases, where you'll drive KOL engagement and regional marketing strategies.
A.P
Acadia Pharmaceuticals
The Director, Medical Science Liaisons (MSL), Rare Diseases leads a high-performing team to implement strategies in the field of rare diseases.
The Associate Director, Commercial Insights and Analytics will provide strategic insights for Arvinas' preclinical and clinical programs.
D.M.T
4D Molecular Therapeutics
4DMT is looking for an experienced intellectual property attorney to manage its IP portfolio and provide strategic legal counsel.
The USP Bioprocessing Specialist III will perform upstream manufacturing and ensure compliance with cGMP regulations in a state-of-the-art facility in New Jersey.
C.P
Centessa Pharmaceuticals
The Director/Sr. Director in Statistical Programming will lead statistical programming efforts and contribute to clinical development in a remote role.