of clinical regulatory medical writing experience #LI-AR1 #LI-Hybrid Pay Range: $136,720 - $205,080 Disclosure Statement... assistance is available. General Summary: The Medical Writing Science Senior Manager is responsible for independently...
: The Medical Writing Science Manager is responsible for authoring & preparing moderately complex clinical and regulatory... documents and represents Medical Writing Science as a cross-functional team member at clinical study level activities. This role...
Job Description Our Medical Writing team at Vertex is in-house, and our Writers are strategic partners in our drug... development process, collaborating with cross functional teams, authoring and driving clinical & regulatory documents to bring...
of Medical Writing Science team responsible for the development of clinical documents, regulatory documents, and scientific...Job Description General Summary: Our Medical Writing function at Vertex is in-house, and our Writers are strategic...
, International QA, Local Market Quality, Clinical Operations, Regulatory and Inspection Readiness teams to drive activities... Establish cross-functional working groups across QA and functional areas in Clinical, Regulatory and manufacturing, including...
and software/tools Own statistical support in the therapeutic areas and/or Global Medical Affairs he/she leads including early.../late clinical developments, post-marketing studies, RWE studies and/or analyses supporting reimbursement Drive innovative...
, On-site or Hybrid ABOUT BMC: At Boston Medical Center (BMC), our diverse staff works together for one goal — to provide... program of its kind in New England. The Research Project Manager (RPM) will oversee and participate in implementing a hybrid...
of clinical trial operations to ensure Vertex trials are conducted in accordance with Good Clinical Practice (GCP) guidelines..., including disposition of intermediates, working cell banks and clinical and commercial drug products internally at Vertex...