Director of Regulatory Affairs

**About Us:**Louisiana Downs Investment Company LLC is committed to providing exceptional gaming experiences for our patrons. We are seeking a highly skilled Regulatory Affairs Specialist to join our team and play a critical role in ensuring compliance with relevant laws and regulations.The estimated salary for this role is $90,000 - $130,000 per year, based...

About BioLife Plasma Services">At BioLife, we are dedicated to transforming patient care through the development of novel specialty pharmaceuticals and best-in-class patient support programs. As a Medical Support Professional at our plasma donation center, you will play a vital role in ensuring the safety and well-being of our donors.">Job Description:">We...

About Evergreen Life ServicesWe strive to make a meaningful difference in the lives of individuals with intellectual and developmental disabilities (IDD). As a charitable, non-profit organization, we aim to provide comprehensive support services tailored to each individual's unique needs. Our team of dedicated professionals works tirelessly to ensure our...

Job DescriptionLouisiana Downs Investment Company LLC is a leading gaming and entertainment company seeking a highly experienced Director of Operations to join our team. As a key member of our leadership team, you will be responsible for ensuring seamless operations, delivering exceptional customer experiences, and driving business growth.About the RoleThis...

Job DescriptionThe Table Games Assistant Manager is responsible for managing all aspects of table games and casino beverage operations.This includes ensuring optimum performance of all areas of responsibility, achieving desired results through staff development and training programs, and maintaining high quality service standards.General Requirements:College...

About the Role:We are seeking a highly qualified Regulatory Affairs Director to lead our compliance efforts at Futu US, Inc.Key Responsibilities:Provide strategic guidance on regulatory matters to ensure compliance with applicable laws and regulations.Develop and implement effective compliance programs to mitigate risks and maintain a strong...

Director/Sr. Director Regulatory AffairsPulmonx is looking for an experienced Director/Sr. Director of Regulatory Affairs to join our dynamic Regulatory Affairs team!* Will consider Sr. Director level depending upon experience.Workplace type: Hybrid (Remote will be considered for candidates in the western US)Responsibilities and Capabilities:Create, lead and...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment...

Why Nuvig Be a part of a potential game-changer for patients with autoimmune disease! Nuvig Therapeutics is developing novel immune therapies to treat a broad spectrum of autoimmune diseases. Our treatments are developed to be active for a broad spectrum of autoimmune diseases, without the inherent side effects and safety concerns of long-term treatment with...

Director / Senior Director, Regulatory AffairsAbout Soleno Therapeutics IncSoleno Therapeutics, Inc., based in Redwood City, California, is a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, including Prader-Willi syndrome (PWS).At Soleno, we are driven by the unique and multi-faceted needs of the PWS...

The Talent Acquisition / HR team manages the recruiting for all positions at Adverum. We only accept resumes from search agencies or recruiters if the Talent Acquisition / HR team has formally requested your help and have a signed agreement in place. Unsolicited resumes sent to Adverum will be considered property of Adverum. The company will not be...

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 + HospitalsMetroPlusHealth provides the highest...

Note to Recruiters and AgenciesThe Talent Acquisition / HR team manages the recruiting for all positions at Adverum. We only accept resumes from search agencies or recruiters if the Talent Acquisition / HR team has formally requested your help and have a signed agreement in place. Unsolicited resumes sent to Adverum will be considered property of Adverum....

Associate Director, CMC Regulatory Affairs- Biologics Job Description The Associate Director, CMC Regulatory Affairs for Biologics is responsible for defining regulatory strategy for one or more molecules in the Biologics portfolio. This position will ensure “right first time” global approvals of CMC regulatory (Biologics) submissions, and “right to...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment...

POSITION SUMMARY The Associate Director, Global Regulatory Affairs provides management of all aspects of assigned regulatory activities for the dedicated regions and related to the development and commercialization of novel liver drugs including quality, preclinical and clinical areas of drug development. This position will manage the timely delivery of...

Associate Director, CMC Regulatory Affairs- BiologicsUnited States - California - Foster CityGilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment...

Director / Senior Director, Regulatory Affairs Labeling, Advertising, and PromotionAbout Soleno Therapeutics IncSoleno Therapeutics, Inc., based in Redwood City, California, is a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, including Prader-Willi syndrome (PWS).At Soleno, we are driven by the...

About the Client:Our client is a global leader in pioneering robotic systems for the diagnosis and treatment of complex medical conditions, with a particular focus on advanced surgical interventions for solid tumors. They are at the forefront of developing cutting-edge technologies and are urgently seeking a highly qualified **Director of Regulatory...

POSITION SUMMARY The Manager, Regulatory Affairs provides support pertaining to regulatory affairs related to the development of novel drugs including preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations. JOB FUNCTIONS/RESPONSIBILITIES Leads preparation of regulatory documentation, in...

Regulatory Affairs EngineerNevro Corp is seeking a highly skilled Regulatory Affairs Engineer to join our team. As a Regulatory Affairs Engineer, you'll be responsible for ensuring that our IT systems and processes comply with regulatory requirements, particularly in the FDA-regulated environment (GxP).You'll work closely with our development teams to...

Job DescriptionAs a Regulatory Affairs Specialist at Axiom Software Solutions Limited, you will be responsible for ensuring compliance with company Standard Operating Procedures and regulatory agency regulations/guidance.Key Responsibilities:Represent Regulatory Affairs on cross-functional project teams.Provide technical expertise to cross-functional teams...

For Current Gilead Employees and Contractors:Please log onto your Internal Career Site to apply for this job.At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access...