Associate Director, IT Medical Affairs Systems - Bridgewater, NJ

We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA submissions and global quality system development. · ...

We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA submissions and global quality system development. · Lead preparation and submission of FDA 510(k) applications. · Coordinate CROs and external consultants. · ...

We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA submissions and global quality system development. · Bachelor's degree in related field. · 5+ years regulatory/quality experience. · ...

We are seeking an experienced Senior Regulatory Affairs & Quality Systems Manager to lead FDA 510(k) and CLIA submissions and global quality system development. · Lead preparation and submission of FDA 510(k) applications. · Coordinate CROs and external consultants. · ...

The job description states that Net2Source, Inc. is one of the fastest growing IT Consulting company across USA. The role of Delivery Lead - Regulatory Affairs involves being the first point of contact for client regional lead and for hub related queries, working in close collabo ...

The Medical Director is responsible for the planning and execution of product-specific scientific/medical strategic and tactical plans. · Responsible for Life Cycle Management Plan development and implementation. · IDentification of product-specific strategic scientific platforms ...

The Medical Director is responsible for the planning and execution of product-specific scientific/medical strategic and tactical plans for a single TA, multiple products or indications. · R&D Point of Contact: Responsible for Life Cycle Management Plan development and implementat ...

The Medical Director is responsible for the planning and execution of product-specific scientific/medical strategic and tactical plans. · R&D Point of Contact Responsible for Life Cycle Management Plan development and implementation. · Serves as medical/scientific subject matter ...

· Recordati Rare Diseases develops high-impact therapies for rare diseases. · ...

We develop and commercialise medicines to serve people living with common diseases as well as those living with some of the rarest in around 150 countries. · This position is with Recordati Rare Diseases Inc RRD North America an affiliate of Recordati. · Recordati Rare Diseases I ...

+ Job summary: Regulatory Affairs Manager is responsible for contributing to and implementing regulatory strategies and tactics for the Company. · + Responsibilities:Act as a primary contact for regulatory affairs on cross-functional product development and post-marketing teams. ...

This position is with Recordati Rare Diseases North America.We are seeking an Associate Training Director Endocrinology to support our commercial organization in developing high-impact training solutions. · ...

You will drive project management and business analysis activities for Life Sciences projects. · Lead end-to-end project management and business analysis activities for Life Sciences initiatives. · Plan, manage, and execute projects to meet agreed-upon scope, timelines, budgets, ...

We are seeking a Vice President to lead our global medical strategy and drive innovation in healthcare. The ideal candidate will have experience in medical affairs and a strong understanding of healthcare systems and policies. · Develop and oversee the global medical TA strategy ...

+This is a Regulatory Affairs position that involves working with a team of Publishers globally. The job requires skills such as good clinical practice and knowledge of regulatory publishing tools. · +Develop/adopt & implement best practices for producing & maintaining high quali ...

This individual will be part of the Global Regulatory Affairs team. · This role assists with planning, writing, compilation,and editing of periodic regulatory reports. · ...

Nestlé Health Science is seeking a Director of Medical Affairs Research to serve as a clinical and health economics expert for microbiome and pancreatic enzyme therapies. · ...

The Associate Training and Development Director Endocrinology will lead the development and execution of training programs for commercial associates in endocrinology. This role requires strong leadership skills, excellent communication abilities, and experience in creating engagi ...

This is a Team Lead – Regulatory Affairs job in Bridgewater. It involves developing and mentoring associates by providing expertise in all submission types applicable to their region of responsibility. · ...

The Associate Training and Development Director Endocrinology hands-on leadership and executional excellence to the function and flawless execution to ensure maximum effectiveness of our field-based associates. · ...