Associate Medical Writer Jobs in USA

Job DescriptionGeneral Summary:The Patient Safety Associate Medical Director will provide medical safety expertise state of the art pharmacovigilance and safety risk management for assigned products (marketed or in development). This role will optimizes patient safety of Vertex products and maintena...

Are you a current UMass Memorial Health caregiver Apply now through Workday.Everyone Is a CaregiverAt UMass Memorial Health everyone is a caregiver regardless of their title or responsibilities. Exceptional patient care academic excellence and leading-edge research make UMass Memorial the premier...

Are you a current UMass Memorial Health caregiver Apply now through Workday.Everyone Is a CaregiverAt UMass Memorial Health everyone is a caregiver regardless of their title or responsibilities. Exceptional patient care academic excellence and leading-edge research make UMass Memorial the premier...

Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatologic...

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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Senior Medical Writer Promotional Review provides high-quality medical review for promotional and non-promotional collateral against local standards best practices and FDA-OPDP requirements. Additionally as part of the M...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionThe Senior Medical Writer - Promotional Review provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject ma...

Site: The McLean Hospital CorporationMass 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 strivin...

Job Title: Process Associate Medical RecordsLocation: Richardson TX (Zip Code: 75023) Work Type: Full Onsite Duration: 6 MonthsPosition OverviewAn organization is seeking detail-oriented individuals for the role of Process Associate Medical Records Transaction Processing. This position involves ha...

Overview/About LumanityLumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product translate the science and data into compelling p...

Overview/About LumanityLumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies around the world to generate evidence to demonstrate the value of their product translate the science and data into compelling p...

Job DescriptionGeneral Summary:The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials working with cross-functional teams on trial strategy design execution and addition to oversight and accountability for the study as a whole this role will serve as...

In order to guard against Phishing Scams please see bottom of Job Description. No outside recruiters/headhunters.The Medical Writer is an entry-level medical content lead for individual accounts and is responsible for the day-to-day development of high quality strategic and scientifically accurate m...

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...