Regulatory Documents Jobs in USA
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Sr. Principal Statistics
Tekwissen Llc
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Job Title: Sr. Principal Statistics Location: Paramus NJ 07652 Job Type: Contract Duration: 6 Months Work Type: Onsit...
Medical Writer
Coopercompanies
DescriptionThe Medical Writer is responsible for developing writing and managing high-quality clinical and regulatory documents that support compliance and product lifecycle needs for global standards such as EU MDR and FDA regulations. This includes planning implementing and reporting clinical data...
Regulatory Affairs Specialist Ii, Animal Health
Thermo Fisher Scientific
Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our cu...
Ophthalmic Technicianvisual Acuity Examiner Part T...
Doctrials
TL;DRPart time position availableAs an Ophthalmic Technician/Visual Acuity Examiner you love working with patients. You are the best of the best when it comes to reviewing detailed study manuals and protocols to perform accurate visual acuity assessments. You are very organized which makes you a per...
Clinical Research Project Manager, Mgb Office Of C...
Mass General Brigham
Site: The Brigham and Womens Hospital Inc.Mass General Brigham relies on a wide range of professionals including doctors nurses business people tech experts researchers and systems analysts to advance our mission. As a not-for-profit we support patient care research teaching and community service st...
Principal Process Engineer Site Based, Redmond, Wa
Evotec
Job Title: Principal Process EngineerAbout Us: this is who we areAt Just Evotec Biologics we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team we thrive on challenging the status quo learning from each other and pushing the boundaries of whats possib...
Global Development Senior Medical Director, Hemato...
Astrazeneca
Job Title: Global Development Senior Medical Director Hematology OncologyHybrid Working: In the office a minimum of 3 days per weekLocation: This Senior Medical Director role is posted in Gaithersburg United States although we are willing to consider candidates in these Hematology locations: Boston...
Bilingual Clinical Research Coordinator
Vanderbilt University Medical Center
Discover Vanderbilt University Medical Center: Located in Nashville Tennessee and operating at a global crossroads of teaching discovery and patient care VUMC is a community ofindividuals who come to work each day with the simple aim of changing the world. It is a place where your expertise will be...
Director, Epidemiology Hepatology
Gsk
Job PurposeThe Global Epidemiology Team provides scientific and strategic leadership in developing and executing real-world evidence strategies to inform drug development across all phases of this role you work across the matrix to support key functions including but not limited to Clinical Develop...
Lead Person Quality Assurance
Rosen's Diversified
OverviewJob Summary The QA Lead is responsible for ensuring product safety quality and compliance on the harvest and fabrication floor through monitoring auditing and documenting any conformities and nonconformities.Key ResponsibilitiesResponsible for overseeing the day-to-day activities for the Qua...
2026 Regulatory Affairs Co-op (6 Months, July 2026...
Gsk
Welcome to Haleon. Were a purpose-driven world-class consumer company putting everyday health in the hands of just three years since our launch weve grown evolved and are now entering an exciting new chapter one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands i...
2026 Regulatory Affairs Co-op (6 Months, July 2026...
Gsk
Welcome to Haleon. Were a purpose-driven world-class consumer company putting everyday health in the hands of just three years since our launch weve grown evolved and are now entering an exciting new chapter one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands i...
Clinical Research Coordinator Ii Grant Funded Card...
Carilion Medical Center
Employment Status:Full timeShift:Day (United States of America)Facility:213 S Jefferson St - RoanokeRequisition Number:R157937 Clinical Research Coordinator II - Grant Funded - Cardiology (Open) How Youll Help Transform Healthcare:The Clinical Research Coordinator will support clinical tria...
Head Of Clinical Sciences
Isomorphic Labs
Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights faster breakthroughs and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A future in which diseases are cur...
Senior Icf Writer (remote)
Mms
About MMSMMS is an innovative data-focused CRO that supports the pharmaceutical biotech and medical device industries with a proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents MMS maintains a 97 percent customer satis...
Fda Regulatory Managing Scientist
Exponent
About ExponentExponent is the only premium engineering and scientific consulting firm with the depth and breadth of expertise to solve our clients most profoundly unique unprecedented and urgent challenges. We are committed to engaging multidisciplinary teams of science engineering and regulatory ex...
Fda Regulatory Managing Scientist
Exponent
About ExponentExponent is the only premium engineering and scientific consulting firm with the depth and breadth of expertise to solve our clients most profoundly unique unprecedented and urgent challenges. We are committed to engaging multidisciplinary teams of science engineering and regulatory ex...
Clinical Trials Manager
Rishabh Rpo
Job Title: Clinical Trials Manager Duration: 12 months Location: Durham NC 27713 (Hybrid- 3 days onsite) Schedule: 8:00 AM to 4:30 PM Job Description Manages clinical trial studies for specific therapeutic area(s). Provides guidance and oversight to internal and external project team member...
Gmp Regulatory Compliance Specialist
Metarpo
REQUIRED: Bachelors required (Masters OK) 26 years experience in Pharma / Biopharma Regulatory compliance and manufacturing Knowledge of GMP. Experience managing authoring of CMC regulatory documents (modules 1.2 2.3 and 3) Must have experience in Veeva Vault RIM - work within RSO ensuring data alig...
Senior Icf Writer (remote)
Mms
About MMSMMS is an innovative data-focused CRO that supports the pharmaceutical biotech and medical device industries with a proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents MMS maintains a 97 percent customer satis...