. General Overview The Human Research Affairs (HRA) Compliance and Education (C&E) Office provides education and support... ethical standards, scientific integrity, and regulatory compliance with ClinicalTrials.gov. This will involve working...
Specialist works cross-functionally in a highly visible position across the Technical Operations group. They will actively... collaborate with research, process development, quality teams, regulatory and CDMOs to ensure a compliant stability program in...
, Regulatory Affairs, Drug Safety, and Medical Affairs. Our products are utilized by 40 out of 50 major biopharmaceutical companies... locations and competitive salaries. Position Summary We are seeking a dynamic and results-driven Marketing Specialist with 2...
Global Market Access & Pricing Specialist - VIE Contract Location: USA, Cambridge Target start date: 01/02/2025... & Pricing Specialist VIE for Dupixent & Itepekimab Respiratory you will support the global market access plan and operation...
research and/or regulatory affairs. Knowledge of federal, state, and local laws and regulations governing human subjects.... General Overview The Expedited Specialist II will conduct reviews of submitted human subject research applications in...
-engineering, Life Sciences, Regulatory Affairs, or related discipline. Master's degree preferred. Minimum of 5-years' experience...As a Medical Device Compliance Specialist, you will play a critical role in helping departments across the company...
and the suffering it causes. A Screening Solutions Specialist (SSS) is a front-line position in the fight against cancer. The... Screening Advocate (SA), Medical Affairs and Marketing. Inform, educate and enable target physician and stakeholder groups...
affairs CROs Regulatory affairs Collaborates with other CRDs within the project, ensures leadership, builds consensus..., Collaborates with functions to ensure full strategic and operational alignment (pharmacovigilance, regulatory...
with internal teams, including Regulatory Affairs, Data Management, and Quality Assurance, to ensure seamless trial execution...Job Description: We are looking for a dedicated Veeva Clinical Operations Specialist to support the management...
regulatory requirements. Therapeutic area is vascular (PVD, CAD, EP) and devices are stents, balloons, guidewires... Affairs. Support, update and maintain the Clinical Trial Management System application for clinical study execution...
Department of Energy Resources Job Description: General Counsel – Program Manager Specialist VIII About DOER The... position of General Counsel, Program Manager Specialist VIII. Job Description DOER’s General Counsel (“GC”) serves as the...
The Assisted Living Certification Unit of the Executive Office of Elder Affairs (EOEA) is responsible for the... certification and regulatory oversight of approximately 271 Assisted Living Residences (ALR’s) statewide. The Registered Nurse...
regulatory requirements. Therapeutic area is vascular (PVD, CAD, EP) and devices are stents, balloons, guidewires... Affairs. Support, update and maintain the Clinical Trial Management System application for clinical study execution...