Fda Submissions Jobs

Foresight Diagnostics is looking for a Clinical Study Manager to oversee and execute clinical trial operations supporting innovative cancer diagnostics.

Drive FDA regulatory compliance and product safety as a Product Regulatory Manager at Dow, a global materials science company focused on innovation and sustainability.

Lead regulatory CMC strategy and submissions for a publicly traded biopharmaceutical company focused on rare diseases.

Lead regulatory affairs for device and combination product submissions at AbbVie, supporting product approvals and strategy development in a hybrid or remote role.

Manage and coordinate medium complexity human subject research projects at Cleveland Clinic to ensure protocol adherence and research compliance.

AbbVie is recruiting an Associate Director, Regulatory Affairs to lead device and combination product regulatory strategies in a hybrid or remote role.

Lead the preparation of clinical regulatory documents at Vertex, a pioneering biotech company, in a hybrid role based in Boston.

Lead global regulatory submissions and strategy for robotic medical devices at Smith+Nephew, driving compliance and product launches across multiple markets.

Contribute your expertise as a Senior Regulatory Affairs Specialist at OrganOx by managing critical regulatory submissions and compliance activities for leading-edge medical device products.

Lead statistical activities for clinical trials in a remote role at Precision Medicine Group, leveraging advanced SAS programming and biostatistics expertise.