Regulatory Affairs Jobs in USA

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesnt just wait for change but actively creates itwhere your skills and valu...

TempOur client City of Houston is in need of a Administrative Specialist. This is a temporary position please see the job details below.Pay Rate: $38.50Schedule: Monday Friday 8am to 5pmLocation: Houston TX 77002 (Downtown Houston)Job Duties:HPD background check must be passed prior to reporting.As...

DescriptionWe are seeking a Clinical Trials and Regulatory Affairs Manager for an exciting opportunity to help launch and establish the Center for Psychedelic Psychotherapy and Trauma Research (the Center) at the Icahn School of Medicine at Mount Sinai in collaboration with its affiliate the James J...

PHMC serves as both a direct service provider to individuals families and communities across the region and as an intermediary agent managing large-scale contracts government and philanthropic partnerships and multidisciplinary initiatives that require operational sophistication strategic leadershi...

We are seeking a highly motivated and detail-oriented Battery Storage Analyst Intern to join our Development team. This role provides an excellent opportunity to gain hands-on experience in grid-connected battery storage projects in several markets throughout the US. The selected candidate will coll...

CuraScript is currently seeking twoLegal Compliance Senior Supervisors. The Senior Compliance Supervisor ensures organizational adherence to all applicable laws regulations and internal policies. This role involves developing and implementing compliance programs monitoring business activities conduc...

Your work will change lives. Including your own.The Impact Youll MakeYou will join an innovative and passionate clinical development team dedicated to improving the lives of patients suffering from devastating diseases. You will lead the innovative clinical pharmacology and pharmacometrics strategy...

Local Study Associate DirectorIntroduction to roleAre you ready to take on a pivotal role in clinical study management As a Local Study Associate Director (LSAD) at AstraZeneca youll lead Local Study Teams to ensure the successful delivery of country-level study commitments. Youll manage clinical st...

Additional Location(s):US-MN-Arden Hills; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling...

Additional Location(s):US-MN-Arden Hills; US-MN-Maple GroveDiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees tackling...

University of Colorado Anschutz Medical CampusDepartment:Cancer CenterWorking Title: Clinical Research Coordinator (Open Rank) GU TeamPosition #: Requisition #: 39190Job Summary:Clinical Science Professionals at all levels perform clinical research related functions which may include patient-orie...

We are seeking an Associate Regulatory Affairs for our North America business. The incumbent will be responsible for maintenance and tracking of regulatory documentation and information pertaining to life cycle management activities; assisting in review of CMC documents for supplements ANDAs NDAs DM...

The R&D Regulatory Affairs Finance team supports the leadership in strategic planning and execution of both current and long-term goals around resource and budget management. This position is responsible for financial planning and analysis related to Plan Update LRP (Long Range Plan) and Latest Best...

The Manager Labeling Regulatory Affairs Strategic Labeling develops and maintains US/EU package inserts and Company Core Data Sheets and coordinates review and approval of these documents with changing regulatory environments. The Manager leads discussions to ensure global consistency of labeling an...

Responsible for assisting with the internal audit system that will assure that all production and support functions at the manufacturing facility operate in compliance with all applicable regulations and standards.ResponsibilitiesAssists with planning and conducting internal compliance audits of all...

Join Sobis mission to improve the lives of people with rare diseases by ensuring the highest standards of product quality and patient safety.As an External Quality Operations Manager (EQOM) youll play a pivotal role in overseeing the quality performance of external manufacturing partners. Acting as...

NPI Engineer Medical Device (Validation & Equipment Qualification)Ultimate Solutions Corp. is a trusted provider of packaging industrial automation serialization and compliance for the Life Science Industries in Puerto Rico United States and Europe. Over a decade the Ultimate team has delivered pro...

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...

Are you ready to steer US promotional regulatory strategy in a way that accelerates responsible growth and earns patient and prescriber trust This role translates science into clear compliant communication across healthcare professionals consumers and payersso that what we say is as strong as the me...

DescriptionSummer Quality/Regulatory Affairs Summer Internship Program offers students the opportunity to gain experience in Public Health Reporting by laboratories to support disease surveillance outbreak detection population health monitoring and regulatory and mandated reporting.This is an Onsite...