Regulatory Affairs Jobs in Rockland, MA

Proclinical Staffing - Boston, MA, United States

Associate Director, Regulatory Affairs - Boston, MA - Permanent Proclinical is seeking a strategic regulatory leader to join a renowned biotech. This is a permanent position located in Boston, MA

from: linkedin.com (+1 source) - 3 days ago

Takeda - Boston, MA, United States

therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Director, Regulatory Affairs

from: linkedin.com - 3 days ago

Biogen - Cambridge, Massachusetts

Job Description Manager, Global Regulatory Affairs About This Role The Global Regulatory Affairs Manager, works closely with Global and Regional Regulatory Leads providing support for a variety

from: resume-library.com - 3 days ago

EPM Scientific - Boston, MA, United States

Title: Senior Director, Clinical Regulatory Affairs Salary : $250,000 to $285,000 Summary: A clinical-stage biopharmaceutical client of ours is seeking a very experienced and motivated person to fill

from: linkedin.com - 9 days ago

ClinCrowd - Waltham, MA, United States

Designs and implements regulatory strategies to obtain and maintain clinical trial applications Experience supporting clinical development...

from: linkedin.com - 3 days ago

Katalyst Healthcares & Life Sciences - Cambridge, Massachusetts

Responsible to communicate new regulatory guidelines. Lead the strategic efforts in the interpretation of relevant and new quality...

from: resume-library.com - 5 days ago

Birdseye Partners - Boston, MA, United States

Our client is seeking a Sr. Director, Clinical Regulatory Affairs to develop regulatory strategies for both non-clinical and clinical programs and lead interactions with regulatory authorities

from: linkedin.com - 11 days ago

Corbus Pharmaceuticals - Norwood, MA, United States

in Regulatory Affairs Experience in all types of regulatory submissions including but not limited to INDs, NDAs, MAA, Type A-D Meetings with FDA, Scientific Advice Consultations with the CHMP of EMA and MHRA, MAA

from: linkedin.com - 9 days ago

Corbus Pharmaceuticals - Norwood, Massachusetts

Overseeing clinical trials submissions performed by Contract Research Organizations (CRO) ensure timely and good quality submissions...

from: resume-library.com - 7 days ago

Cellarity - Somerville, MA, United States

in a revolutionary way? What if you could be the first hire in Regulatory Affairs with the opportunity to build a strategy and your team as we expand our clinical pipeline? What this position is all about : Cellarity

from: linkedin.com - 9 days ago