Biotechnology Research Jobs in USA

Roles & Responsibilities1. Implementation and continuous improvement of the Medical Device Quality2. Management Systems and associated CE requirements in order to meet customer3. and regulatory requirements 4. Preparation implementation and Maintenance of Manual policies work instructions as per ISO...

Purpose:The Senior Director Global Training Strategy & Effectiveness is responsible for designing and executing a world-class global training program and organization within Operations globally. This leader will set the vision and framework to build an integrated and aligned training capability that...

Job Description Contact: Alexandra Spink - No 3rd party candidatesWe are seeking an experienced Regulatory Medical Writer to provide fractional support for the development of complex regulatory submission documents. Requires a writer who can lead document strategy...

Do you want to leverage your electric industry knowledge and persuasive writing skills LCRA is looking for a proactive Regulatory Case Manager Lead to bolster our advocacy work for our transmission and wholesale power businesses. This high-level role entails overseeing regulatory projects contested...

Government & Regulatory Affairs - Trade Remedies Associate About the Role: As an Associate in the Trade Remedies group you will work on complex trade matters involving investigations administrative proceedings and litigation. The role offers significant hands-on experience and the opportunity...

As a Principal Medical Writer you will provide communication expertise and lead a strategy-driven approach to authoring of key clinical and regulatory documents and regulatory submissions to ensure clarity credibility and consistency of clinical information throughout submission packages and clinica...

The Associate Director Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials patient safety and global medical affairs. The Associate Director works in partnership with expert...

The Associate Director Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials patient safety and global medical affairs. The Associate Director works in partnership with expert...

SkyBridge Tactical is a Prime Contractor for MSOFS and a Service Disabled Veteran Owned Small Business (SDVOSB) headquartered in Tampa FL founded in 2008 to support our customers global security operational and training needs focusing on mission success in most challenging environments. SBT current...

Role SummaryIntegrity Alliance is a dualregistrant FINRA member brokerdealer and SEC-registered investment adviser with a multistate footprint. The Regulatory Manager will own day-to-day execution of our regulatory program across the BD and RIA including state registrations and licensing FINRA/SEC/S...

Job Summary:The Director of Regulatory Affairs is responsible for executing the companys regulatory strategy across the development and commercial product portfolio. This role reports to the Senior Vice President Regulatory Affairs. This individual serves as the regulatory affairs main contact to pr...

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

Do you want to leverage your electric industry knowledge and project management skills LCRA is looking for a proactive Regulatory Case Manager Lead to bolster our advocacy work for our transmission business. This expert-level role entails overseeing Certificate of Convenience and Necessity (CCN) ame...

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...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

Application close date:Applications will be accepted on an ongoing basis until the requisition is closed.At Blue Origin we envision millions of people living and working in space for the benefit of Earth. Were working to develop reusable safe and low-cost space vehicles and systems within a culture...

DescriptionThe Prudential Regulatory Affairs team is tasked with leading strategy on all proposed prudential regulatory policy initiatives affecting relevant JPMC lines of business. The global public policy environment is evolving rapidly driven by technological change evolving and emerging risks an...

Title: Manager Faculty Affairs & DevelopmentDepartment Org: Faculty Affairs - 107880Employee Classification: J1 - Salaried Full Time HSCBargaining Unit:Professional Staff AssociationPrimary Location: HSC SShift:1Job Description:This role supports the Associate Dean and the Director of the Office for...

DescriptionJOB SUMMARYThe Senior Director General Manager (GM) Development serves as the enterprise leader and architect of Marriotts global General Manager Development strategy. This role is accountable for defining governing and continuously evolving a comprehensive end-to-end GM Development Ecosy...

OverviewSince our founding in 1924 weve cut cardiovascular disease deaths in half but there is still so much more to do. To overcome todays biggest health challenges and accelerate this progress we need passionate individuals like you. Join our movement be part of the progress and help ensure a heal...