Regulatory Specialist
Stanford University
Stanford University’s Division of Pulmonary, Allergy, and Critical Care Medicine (PACCM) invites applications for a Clinical Trials Regulatory Specialist (CTRS). This remote, full-time role supports regulatory oversight across diverse clinical research projects, including industry-sponsored, NIH, and PI-initiated trials as well as observational registries.
The CTRS provides regulatory expertise to ensure compliance with University and external policies, coordinating submissions and
#J-18808-LjbffrVacancy posted 7 hours ago
Similar jobs that could be interesting for youBased on the Regulatory Specialist in United States vacancy
- ...Job Description Job Description EHS, QMS & Regulatory Specialist Specialty Chemical Manufacturer | Carlstadt, NJ | Full-Time, On-Site About the Role Our client, an established specialty chemical manufacturer, is looking for an EHS, QMS & Regulatory Specialist...SuggestedFull timeLocal area
Synerfac Technical Staffing
Carlstadt, NJ1 day ago - The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan, create, develop and maintain materials needed for regulatory compliance...Suggested
- ...notifications.• Participate in team meetings as a representative of IA with both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical reports.• The candidate must be able to adhere to local and global...SuggestedWork at officeLocal areaImmediate start
- ...approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.A Regulatory Affairs Specialist II position is available in the Diamond Research Laboratory. You will assist and support internal and external PIs, for...SuggestedWork experience placement
$107.2k - $160.8k
...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and...SuggestedWork at officeLocal areaImmediate startFlexible hours- ...is working in the CMC area. Relevant experience is requiredExperience: 3 to 6 yearsExperience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience )Scientific background,Required Skills:CMC/ Regulatory writing experienceScientific...Work at officeImmediate start
- .../financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...Work at officeImmediate start
- Job-ID31525652Reference25-04486 Responsibilities: The Regulatory Affairs Specialist is responsible for working with cross-functional teams to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality...
- Job-ID29247439Reference25-02134 Responsibilities: Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic submissions. Leader in the development of dossiers for registration of products in countries outside the US; including...Work at office
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...Immediate start
- ...Manufacturing, and/or Project Management within the IVD industry. Knowledge of FDA, and CE marking requirements for IVD products is preferred. Excellent verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
- Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This role is responsible for ensuring compliance with...
- The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and...
- ...solutions, and safeguarding people, property, and profits. Position Summary The Compliance Associate supports RPM Living’s regulatory compliance program across property operations. This role assists with monitoring regulatory developments, maintaining compliance...Weekly payFull timeStart working todayWork at officeLocal area3 days per week
- The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the... ...basis.Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. Manage compliance...Contract work
- Job-ID31596302Reference25-04614 Job Description: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe, support of international product registrations and related regulatory affairs activities...Work at office
- ...processes, policies, and people delivering value. Learn More About ProSidian Consulting at DescriptionProSidian Seeks a Regulatory Compliance Specialist | Compliance / Risk / Regulatory: Risk, Compliance & Independent Certification Support [DOE0019019] for Program...Full timeContract workTemporary workFor contractorsWork at officeLocal areaRemote workFlexible hours
- Brecksville, OHDescriptionJob Title: Regulatory Affairs SpecialistDepartment: RegulatoryReports To: Director of Regulatory AffairsFLSA Status: ExemptSupervise the work of others: NoPosition Summary:This position is responsible for preparing submissions to various regulatory...Work experience placementWork at office
- Job-ID29095910Reference26-23457Remote50% Remote Experience • 3-5 years of experience in regulatory compliance, information security, and/or data privacy • Demonstrated experience working within cross-functional teams including Legal, IT, Security Operations, and Governance...Remote work
$120k - $160k
...members to perform at a higher level through a deep understanding of their bodies and daily lives.WHOOP is looking for a Regulatory Affairs Specialist II, Expansion to be a core member of the Digital Health team.As the Regulatory Affairs Specialist II, Expansion, you...Full timeWork at officeRelocation$71.6k - $119.3k
...Meet the team: Regulatory Affairs is a team of more than 40 professionals located either at San Diego HQ or remotely around the globe. Our backgrounds range from biological and physical sciences to engineering, political science to biostatistics, pharmacology to law just...Work at officeRemote workHome officeFlexible hoursDexcom
San Diego, CA2 days ago$74.4k - $111.6k
...functional collaboration as we work together to engineer the extraordinary. This position will be based in Mounds View, MN. The Regulatory Affairs Specialist assists in the development of strategies for worldwide product registration with global regulatory agencies to introduce...H1bLocal areaRemote workWorldwideFlexible hoursMED Medtronic Inc
Minnesota1 day ago$74.4k - $111.6k
...healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Medtronic is seeking a Regulatory Affairs Specialist to support the Wound Management Regulatory Affairs team. The selected candidate will provide regulatory support on a...Full timeH1bWork at officeLocal areaImmediate startFlexible hoursMedtronic
North Haven, CT13 hours ago- ...Regulatory Affairs Specialist Our client, a Medical Devices/Healthcare company, is looking for a Regulatory Affairs Specialist for their Warsaw, IN location. Responsibilities: Responsible for assisting the team with regulatory filings as necessary to market client...Work at office
ICONMA
Warsaw, IN2 days ago - ...Regulatory Affairs Specialist The Regulatory Affairs Specialist is responsible for supporting the development, execution, and maintenance of regulatory strategies to ensure compliance with applicable global regulations for medical devices. This role will play a critical...Local area
Urgomedical
Fort Worth, TX1 day ago - ...Regulatory Affairs Specialist II The Regulatory Affairs Specialist II supports regulatory submissions and regulatory authority interactions related to product submissions and approvals. In this role, you will prepare and submit regulatory documentation, support product...
Anika Corporation
Bedford, MA1 day ago - ...Job Title : Regulatory Affairs Specialist/Food Safety & Quality Manager Location : Columbus, OH 43219 Duration : 10 Months Education : Bachelor Degeee Job Description Please focus on applicants with quality background and specifically people with experience in reading/...Work experience placement
ProKatchers
Columbus, OH3 days ago - ...Company: Synergy Spine Solutions Inc. Reports to: Vice President, Regulatory Affairs & Quality Assurance About Synergy Spine Solutions... .... About the role We're seeking a mid-level Regulatory Affairs Specialist to support the global regulatory lifecycle of the Synergy Disc...
Synergy Spine Solutions
Louisville, CO3 days ago - ...DreamBone® and SmartBones®. Job Summary Join a team that helps bring innovative products to market while ensuring they meet regulatory requirements worldwide. In this role, you'll support new product development, safety data sheet maintenance and authoring, and...Work at officeWorldwide
Spectrum Brands
Saint Louis, MO2 days ago - ...Working Together, Persist with Passion. Who We’re Looking For: Laborie Medical Technologies is currently searching for a Regulatory Affairs Specialist to join our team in a hybrid role based out of the Portsmouth, NH or Minnetonka, MN offices. The Regulatory Affairs...WorldwideFlexible hours
Laborie Medical Technologies Corp
Minnetonka, MN2 days ago
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Specialist. Be the first to apply!
Related searches
- compliance analyst United States
- tax compliance analyst United States
- quality compliance specialist United States
- junior regulatory affairs specialist United States
- regulatory compliance specialist United States
- product compliance specialist United States
- junior compliance analyst United States
- regulatory affairs specialist United States
- compliance data analyst United States
- legal compliance analyst United States