Regulatory Affairs Consultant - United States - Newton - Massachusetts

Parexel International LLC seeks a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials. The position may telecommute from anywhere in the United States up to 5 days per week. · ...

We are seeking a Regulatory Affairs Consultant to prepare clinical and regulatory documentation for clinical trials and deliver consulting services to ensure that the company meets regulatory requirements. · ...

We are seeking an experienced Regulatory Consultant to independently lead regulatory projects and deliver high-quality, pragmatic regulatory advice to clients across the US, EU, and UK regulatory landscapes.The opportunity involves leading smaller regulatory projects end-to-end a ...

Contribute to strategic and operational regulatory planning Author sections of the Investigator's Brochure (IB) and manage electronic submissions Collaborate cross-functionally with the program manager and CSO on deliverables leading up to IND. · ...

This is a fully remote opportunity for Regulatory Affairs Consultant with strong regulatory writing experience and background in autoimmune or inflammatory disease and biotech environments. · ...

As part of the BME Strategies Management Team, · the Managing Consultant plays a pivotal role in shaping the firm's strategic direction in public health communications. · The PA Practice Lead will guide strategy and lead high-quality technical assistance projects related to publi ...

BME Strategies is a consulting firm that specializes in providing public health design and implementation programming for local, regional, and state governments. · Key Responsibilities · Develop and execute End-to-end Campaign Planning & Execution. · ...

The Surgical Pathology Coordinator will be responsible for registering and verifying consult cases received by the Pathology Service. · ...

Responsible for registration insurance verification consult cases received by Pathology Service accessioning specimens approved protocols Documentation materials received consult cases Will work under general supervision perform clerical technical functions required core front-en ...

Reporting to the Chief People Officer, the Director, Human Resources Business Partner (HRBP) provides HR leadership and consultation to client groups within multiple functions. · ...

We exist to change our patients' lives through the power of sight.We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology. · ...

The Director, Human Resources Business Partner provides HR leadership and consultation to client groups within multiple functions. They are a trusted advisor to leaders, providing expert HR advice and advanced solutions that enable the achievement of business strategies. · Provid ...

Be Seen and Heard at EyePoint · We See You. · Award-winning approach in business fuels our focus on science and innovation to offer a lifetime of clearer vision · ...

Nuestro cliente en Waltham está buscando agregar un contrato para Medical Affairs Ops para apoyar los procesos administrativos, contractuals y financieros del equipo. · ...

+The Regulatory Affairs Specialist US is responsible for preparing regulatory submissions and documentation required for U.S. FDA approvals of high-risk medical devices. · +Bachelor's degree in Regulatory Affairs or related field · Around 3–5 years of regulatory affairs experienc ...

Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medicines that meet significant unmet medical needs. · ...

The Director, Regulatory Affairs will be responsible for the strategic leadership, · development and execution of science-based, solution-oriented, · and globally aligned regulatory strategies for the program(s) · under his/her accountability.This role serves as a key · regulator ...

Our client is seeking a Pharmacovigilance Operations Manager to support global safety case management. · ...

The Senior Director of Regulatory Affairs will develop and execute global regulatory strategies in collaboration with key stakeholders.You will serve as the global regulatory lead for our multifocal motor neuropathy (MMN) program and support other programs as needed, providing ex ...

As C4T's Vice President, Investor Relations & Communications, you will lead our external investor strategies and communications activities, · ensuring consistent messaging across all platforms to all stakeholders. · Lead the strategic planning, direction, and execution of IR/PR/C ...