Medical Writer Jobs in USA

Job DescriptionUW Medicine Strategic Communications has an outstanding opportunity for a Senior Writer to join their team.About this OpportunityReporting to the Director of Internal Communications the Senior Writer is responsible for creating compelling executive and organizational communications th...

Introduction:Xencor is a public clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego. Our focus is developing high-potential XmAb bispecific T-cell engagers and additional engineered drug candidates that leverage our differentiated technology platforms...

Introduction:Xencor is a public clinical-stage biopharmaceutical company located in the Los Angeles area (Pasadena) and in San Diego. Our focus is developing high-potential XmAb bispecific T-cell engagers and additional engineered drug candidates that leverage our differentiated technology platforms...

Castle Biosciences Earns Top Workplaces USA Award for Phoenix Pittsburgh and Friendswood! Learn more at Castle Biosciences Inc. is growing and we are looking to hire a full-time Medical Writer working from our Friendswood TX headquarters (preferred) or Pittsburgh PA @ Nova Place office location wit...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing to life our Mission: enabling our customers to make the world healthier cleaner and s...

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Clinical Research Coordinator to interact directly with our healthy volunteer participants while learning to read clinical research protoco...

Job Title Senior Clinical Evaluation Medical Writer Job Location Type Remote Job Type 24-Month Contract (Potential Temp-to-Hire) Shift Schedule 1st Shift Standard Business Hours About the Role We are seeking an experienced Senior Clinical Evaluation Medical Writer to support clinic...

Job DescriptionThis position drives scientific planning strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead you will collaborate with global cross functional team members including clinical directors and study managers to lead/support clinical trial scientif...

Job DescriptionThe Associate Director Global Scientific & Value Content - Payor (AD GSVC-Payor) position resides in the Value & Implementation (V&I) organization which includes Global Medical and Scientific Affairs and Outcomes Research. The AD GSVC- Payor is a mid-level role that reports directly i...

ROLE SUMMARYThe Clinician Medical Monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design execution monitoring delivery and reporting of one or more clinical studies and to ensure patient safety...

As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking an Clinical Research Coordinator Assistant to interact directly with our healthy volunteer participants while learning to read clinical resear...

ROLE SUMMARYThe Clinician Medical Monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design execution monitoring delivery and reporting of one or more clinical studies and to ensure patient safety...

Experience level: Mid-senior Experience required: 5 Years Education level: Doctorate Job function: Health Care Provider Industry: Pharmaceuticals Total position: 1 Relocation assistance: No Visa sponsorship eligibility: NoSUMMARY OF POSITION: We are seeking a skilled Medical Writer to develop high-q...

ROLE SUMMARYThe Clinician Medical Monitor is accountable for providing medical and scientific expertise and oversight for Clinical Trials and serves as a single point of accountability for design execution monitoring delivery and reporting of one or more clinical studies and to ensure patient safety...

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...

DescriptionThe Senior 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 clinic...

Job DescriptionContact: Alexandra Spink - No 3rd party candidatesOur client is seeking a Medical Writing Editor to support quality control (QC) review copyediting and submission readiness for clinical and regulatory documents. This role partners with Medical Writers and cross-functional teams to ens...

Trilogy Writing & Consulting anIndegenecompanyis currently looking to hireaMedical WritingManager/Senior Manager reporting directly to the Director of Medical Writingto support our growing company in producing regulatory documentation for the international pharmaceutical industry. At Trilogy you wil...