Director of Regulatory Affairs Strategy

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal...

Job DescriptionJob DescriptionScismic is supporting the growth of a late-stage, publicly traded biopharmaceutical company developing targeted radiotherapies to deliver cancer-killing radiation with cellular level precision to treat patients with high unmet medical needs.  Their vision is to build a specialty, hospital-focused radiotherapeutics company that...

Overview: Director of Compliance and Regulatory Affairs Overview   The primary function of this position is to direct and provide oversight of Somnia’s Compliance and Regulatory Affairs Program.  The individual will be responsible for planning, implementing, and managing a compliance and regulatory affairs program for Somnia and its affiliated...

Director, Regulatory Affairs, Advertising and Promotion (Ad/Promo) Remote – United States Seeking a Director of Regulatory Affairs for Advertising and Promotion to lead commercial regulatory strategy and leadership for the US business for a commercialized biopharmaceutical focused on Oncology. This new hire will ensure compliance in US marketing activities...

VP of Regulatory AffairsI am partnered with a scientifically driven late-stage, well funded biopharmaceutical company who are looking to build out their Solid Tumors pipeline. They are looking for a Vice President of Clinical Regulatory Affairs to be responsible for the development and execution of the company regulatory strategy, serving as global...

Regulatory Affairs Regulatory Affairs SME Compensation: $110,000 to $130,000 Location: Shelbyville, IN ABOUT OUR CLIENT: Our client is a leader in their space, in SE Indianapolis. Their state-of-the-art facility will be where groundbreaking ideas become reality. Their contracts unrelated to automotive will provide long term stability. As a leading player in...

About the OpportunityOur client is a growing biopharmaceutical company in need of a Sr. Manager/Associate Director of Regulatory Affairs Strategy to join their team. This role is responsible for developing, implementing, and leading short/long term global regulatory strategies that support the success of their pharmaceutical products.The annual base salary...

Regulatory Affairs Consultant Cambridge MA, Remote with occasional site time Medical Device 6 month contract - 40 hours per week Competitve hourly rate A MedTech company based in Massachusetts specializing in Class 2 Medical Device solutions are looking to hire a contractor for a 6-month renewable contract to support with product submissions in multiple...

My client are looking for a Regulatory Affairs Specialist with experience in Asia Pacific Product Registrations. You MUST be willing to work hybrid in office at Exton, Pennsylvania. Essential Duties and Responsibilities: Author and review China, South Korea, Japan and additional submissions as well as US and EU Submissions Work cross functionally with...

. The Director of the Regulatory and Strategic Program Management team is responsible for driving the successful implementation of the firms key regulatory and strategic initiatives and related strategies, partnering with stakeholders across the ent Director, Regulatory, Management, Program, Strategic, Regulatory Affairs, Business Services

Our customer is looking for a Senior Regulatory Affairs Specialist to join a team of 7 and supporting the product submissions, regulatory guidance, and registering products. Duties Include: Maintain and establish regulatory functions for medical device and environmental compliance. Uphold Quality Management System for domestic and international...

Job Title: Senior Regulatory Affairs Specialist Duration: 9 months Location: Irvine, CA (Onsite) Shift: 8 am to 5 pm. Our Client is a Global medical device Manufacturer. We are looking for a Senior Regulatory Affairs Specialist to complete and maintain regulatory approvals and clearances of assigned products. Create regulatory submissions (exercising...

Job DescriptionJob DescriptionScismic is supporting the growth of a late-stage, publicly traded biopharmaceutical company developing targeted radiotherapies to deliver cancer-killing radiation with cellular level precision to treat patients with high unmet medical needs.  Their vision is to build a specialty, hospital-focused radiotherapeutics company that...

We believe that great healthcare is an essential safeguard of human dignity. At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers...

The Company is a Pharmaceutical company that has a great underdog story. They started as a generic company until they hired a new CEO who has turned the company around. They went from struggling to now 3x their stock. Their main focus is on women's health. Join our team as a Director Regulatory Affairs, reporting directly to the Vice President of Regulatory...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...

Lead the regulatory efforts for IND-enabling activities, including the preparation of the Investigational New Drug (IND) application for our groundbreaking oncology and CNS therapies targeted for submission this year and early next.Be the go for all things regulatory and acting as a key voice to the future of all trials, SOPs and strategy for these early...

Overview: Undergraduate or Graduate student in a Science discipline.  This individual will work in our Regulatory Affairs Department, supporting the Regulatory Strategy group.  He/she will be assigned interesting and challenging projects related to competitive data research, precedent analysis, regulatory environment monitoring and ad hoc projects. ...

**Empower. Unite. Care.**: **MetroPlusHealth** is committed to empowering New Yorkers by uniting communities through care. We believe that Health care is a right, not a privilege. If you have compassion and a collaborative spirit, work with us. You can come to work being proud of what you do every day. **About NYC Health + Hospitals**: MetroPlus**Health...