Regulatory Submissions Jobs in USA

Make your mark for patientsTo strengthen ourNon-Clinical Safety Evaluation group within Early Clinical Development and Translational Science we are looking for a talented individual for the role of Non-Clinical Safety Lead based inCambridge MA (USA)About the roleAs a Non-clinical Safety Lead you wil...

The Role:We are seeking a proactive and experienced Regulatory Affairs Manager to lead and coordinate global regulatory activities supporting the development of our biologic therapeutics. This role will independently manage key submission components contribute to regulatory strategy and help drive c...

DescriptionAre you passionate about tackling difficult questions using data to drive insights and looking for the opportunity to support industry-leading businesses with your analysis As a member of the Corporate and Investment Bank (CIB) Treasury Deposit Analytics team you will play a role in aidin...

DescriptionDiscover a Technology career with real meaning. One that offers the opportunity to showcase your talents achieve measurable success and gain immense satisfaction by enabling healthier lives everywhere every day.The Senior Systems Engineer is a senior individual contributor responsible for...

Associate Director/Director Commercial Project ManagementSkyhawk Therapeutics is seeking a highly motivated and experienced Associate Director Commercial Project Management to lead cross-functional planning and execution for the launch of SKY-0515 a potential first-in-class disease-modifying therap...

Job Description About Allogene:Allogene Therapeutics with headquarters in South San Francisco is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management t...

The Manager Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality preclinical and clinical areas of drug development and the policies/procedures req...

Manager Regulatory Affairs at Helen of Troy Nevada Corporation in Marlborough MAManage regulatory requirements for new projects and changes to existing products. Work with cross-functional team consisting of engineering marketing and quality to develop regulatory plans for key consumer products for...

Job Title: Provider Network Manager Department: Network ManagementAbout the Role: The Provider Network Manager is responsible for managing and optimizing assigned segments of the provider network in San Fernando Valley to ensure adequate access strong provider performance and alignment with organiza...

Job Title: Provider Network Manager Department: Network ManagementAbout the Role: The Provider Network Manager is responsible for managing and optimizing assigned segments of the provider network in San Fernando Valley to ensure adequate access strong provider performance and alignment with organiza...

JOB SUMMARYThe Global Development Lead (GDL) represents Clinical on the Global Medicine Team and is the single clinical point of accountability for clinical development for assigned asset(s) in Internal Medicine Research & Development Pfizer. The individual will lead the cross-functional Clinical De...

We seek to move the world forward through innovative thinking.Woolpert is an award-winning global leader in architecture engineering and geospatial services. We blend design excellence with cutting-edge technology to deliver exceptional client value. Our team is passionate about their work and commi...

Make a meaningful difference to patients around the world. From design to production our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory environments. Working in partnership with external government and regulatory authorities and...

Job Description SummaryThe Principal Manufacturing Scientist is a Subject Matter Expert (SME) in radiopharmaceutical manufacturing and radiochemistry. The role acts as global technical product owner for PET radiopharmaceuticals manufactured on the FastLab platform with endtoend accountability from l...

DescriptionAre you passionate about patient safety and ready to help lead a fast-paced global pharmacovigilance organization Ascendis Pharma is seeking an experienced Program Safety Lead to champion safety excellence drive compliance and shape strategy across our growing portfolio.We are a dynamic g...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Hourly Pay Range:$24.86 - $37.29 - The hourly pay rate offered is determined by a candidates expertise and years of experience among other factors.Position HighlightsPosition: Research CoordinatorLocation: Evanston ILFull Time/Part Time: Full TimeHours: Monday-FridayRequired Travel: possible travel...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

DescriptionTitle: Clinical Research Scientist Status: ExemptLocation: Onsite San Clara CA Reports to: Vice President of Clinical AffairsAbout the Company VahatiCor is developing next-generation intravascular technologies designed to improve outcomes in cardiovascular care. As an early-stage company...

DescriptionTitle: Product Development Manager - Advanced NanoTherapiesStatus: ExemptLocation: Onsite Cleveland OHReports to: VP of Research and DevelopmentAbout Advanced NanoTherapiesAdvanced NanoTherapies (ANT) a portfolio company of T45 Labs is a clinical-stage medical device company developing ne...