Regulatory Affairs Consultant - Boston

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. · ...

· Founded in 2004, BME Strategies is a mission-driven consulting firm specializing in providing Public Health design and implementation programming for local, regional, and state governments. · Position Overview · As part of the BME Strategies Management Team, the Managing Consu ...

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 all share the same goal - to improve the world's health. · ...

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. · ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

Overview/About LumanityLumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product, translate the science and d ...

A global health consulting firm in Boston seeks a Principal Consultant to deliver key Medical Affairs projects and foster business growth. · All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description. · The ...

Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. We partner with our clients to navigate complex challenges, unlock the full value of their assets, and shape the future of medicine. · ...

We are seeking an exceptional individual with a track record of success in life sciences strategy consulting and a deep interest in Medical Affairs.You will be responsible for the successful delivery of complex strategic engagements across a range of Medical Affairs related proje ...

· Overview/About Lumanity · Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner that brings together strategy, evidence, engagement, and technology, we were designed to engineer breakt ...

Contract: [[cust_TypeOfContract]] · Compensation: [[salaryMin]] · If you've worn a pair of glasses, we've already met. · We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in over 15 ...

The GMP Operational Quality Senior Manager at Stark Pharma will oversee and ensure compliance with Good Manufacturing Practices within manufacturing and quality assurance processes. · Strong knowledge of GMP, Quality Assurance practices, and Validation processesExperience with re ...

Antares Therapeutics is seeking an experienced Regulatory Affairs–CMC Strategist (Consultant) to provide senior strategic advisory leadership for global, phase-appropriate CMC regulatory strategies supporting early-stage small molecule product development. · Advanced degree (PhD, ...

· Company Description · At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We're fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is committed to creating and delivering next-generation commerci ...

Hartman Young is working with an innovative biotech oncology company to support the appointment of a Pharmacovigilance (PV) Consultant. · ...

The GMP Operational Quality Senior Manager at Stark Pharma will oversee and ensure compliance with Good Manufacturing Practices (GMP) within manufacturing and quality assurance processes. · ...

Job summary · Rios Partners is a mission-driven consulting firm committed to creating positive impact by delivering value for our clients, · investing in our people, and solving tough problems that strengthen our local, national, and global communities. · ...

Contract: · [[cust_TypeOfContract]] · Compensation: · [[salaryMin]] · If you've worn a pair of glasses, we've already met. · We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in ove ...