Associate Director, Regulatory Affairs ROW - Princeton

The Associate Director Regulatory Affairs ROW is responsible for building and executing global regulatory strategy objectives policies programs pertaining to development marketing Acadia products including regulatory compliance advertising promotion marketed products. · ...

The Associate Director will be responsible for helping build and execute global regulatory strategy objectives policies and programs pertaining to development marketing Acadia products including regulatory compliance for advertising promotion marketed products. · This role will s ...

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe and the United States. Today we're advancing programs in Endocrinology Rare Disease and Oncology. · The Regulatory Project Manager will be an integral part of Global Regu ...

+Job summary · Ascendis Pharma is a dynamic biopharmaceutical company advancing programs in Endocrinology Rare Disease and Oncology. · +ResponsibilitiesProvide project management leadership to global regulatory submissions. · Collaborate with cross-functional teams to ensure deli ...

+ Inspection Readiness Lead at Made Scientific:JOB SUMMARY+ The Inspection Readiness Lead (Associate Director) is responsible for establishing, maintaining, and continuously improving a state of inspection readiness across GMP cell therapy operations.+ · + ++Design, implement, a ...

The Inspection Readiness Lead (Associate Director) is a quality leader responsible for establishing and maintaining inspection readiness across GMP cell therapy operations from clinical through commercial stages. · Design, implement and sustain multi-site inspection readiness pro ...

+The company is looking for a Medical Writer III to work on medical writing projects and activities across therapeutic areas. The primary responsibilities include leading key medical writing projects and preparing scientific and regulatory documents related to the clinical develo ...

+Job summary:The primary responsibilities of an Associate Director Medical Writer at client include, but are not limited to, leading key medical writing projects and activities across therapeutic areas and preparing (under minimal supervision) scientific and regulatory documents ...

This is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally. · Maintains therapeutic area and product knowledge through ongoing assessment of relevant ...

The designer will join the company team responsible for supporting Corporate Affairs business communications.Primary responsibilities are related to the development and distribution of internal and external communications, working with CA creative director and content team. · ...

Clinical Trial Lead will be responsible for driving the development and execution of deliverables for assigned Medical Affairs Sponsored Trials (MAST) · Ensure high quality and timely execution of key deliverables and maintain data integrity · Accountable for ensuring scientific ...

Content management specialist job summary: · We are looking for a content management specialist to support the integration and transition of markets to new workflows and provide system administrative support including onboarding of new users to the content management systems. · ...

The Established Brands medical scientist-contractor is responsible for the medical oversight of activities for brands in late stages of life cycle and those which have undergone Loss-of-Exclusivity.Provide medical input to patient safety monitoring of the brand and available lite ...

We are seeking a Scientific Global Regulatory Manager to support our team in the preparation of HA interactions and maintain tracking data for health authority meetings. · Support Regulatory Lead in the preparation of HA interactions (meeting preparation, rehearsals, execution, f ...

We believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value. · We want you to fit in with an inclusive culture, focus on work-life fit and well-being, and a supportive, connected environment; but we also want you to s ...

The Regulatory & Medical Affairs - Promotional Review Advisor will have the opportunity to serve as a strategic partner who is solutions oriented and focused on ensuring medical accuracy and scientific validity of promotional communications with robust scientific evidence and com ...

Provides support activities and assists with the workflow for specific tasks on document publishing requests between Client and our service providers; works closely with both service providers and Client teams to communicate priorities for document publishing. · ...

This position is responsible for the supply planning and inventory management of clinical supplies required to support global clinical research and development studies during phases 1-4. Collaborating with internal and external Customers and Service Providers including but not li ...

We are seeking a Medical Scientist/Medical Monitor to join our team at Net2Source Inc. · The Established Brands medical scientist-contractor is responsible for the medical oversight of activities for brands in late stages of life cycle and those which have undergone Loss-of-Exclu ...

We are seeking a Global Regulatory CMC Manager to join our team! As a key member of our regulatory affairs team, you will be responsible for developing and implementing global regulatory strategies for post-approval small molecule product submissions. · Participate in the develop ...