- Parexel (Dover, DE)
- The Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the ... of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and...projects. **Training/Compliance** + Keep abreast of new advances in medical writing and regulatory issues. + Develop… more
- Parexel (Madison, WI)
- **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting ... by Medical Writing Support Coordinator, Document Specialist, and/or Associate Medical Writer for assembly of project files and client deliverables.… more
- Merck & Co. (Durham, NC)
- …determine product dispositionPreparing and/or providing guidance and review for regulatory filings, process descriptions, investigations, and change requests. Acts ... as a participant in domestic and international regulatory agency inspectionsSupporting all quality and safety initiativesProvide technical support to manufacturing… more
- ThermoFisher Scientific (Greenville, NC)
- …(Mon-Fri) **Environmental Conditions** Office **Job Description** **FSP Senior** ** Regulatory ** ** Medical Writer (** ** Remote ;** **US** **)** At Thermo ... are seeking candidates based in the US! As a remote -based Senior Medical Writer within...possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases… more
- Terumo Neuro (Aliso Viejo, CA)
- **12933BR** **Title:** Sr. Medical Writer (US Remote & Temp to Hire) **Job Description:** **INNOVATION STARTS WITH YOU** Are you interested in working for an ... of regulatory / clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or ...and San Francisco Fair Chance Ordinance. **External-Facing Title:** Sr. Medical Writer (US Remote &… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Principal Medical Writer Associate Director **Location** : USA, Remote . Proximity to Cambridge/Boston, MA or Morristown, NJ is highly ... serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and...**About You** **Core Experience** : + Six+ years as medical writer or equivalent specialist role +… more
- Flywheel Partners (New York, NY)
- …trust + Professional Development + Learn the Flywheel pathways for advancement within the Medical Writer track, or other roles based on interest and capabilities ... in scheduled status calls and client review meetings with Medical , Marketing, Sales, Legal, and Regulatory +...manage focus, communication, and the necessary workload in a remote environment Salary Range: $80K - $85K per year.… more
- Adecco US, Inc. (Morristown, NJ)
- Adecco Healthcare & Life Sciences is seeking a skilled **CMC Regulatory Technical Writer II** to support a global pharmaceutical client in lifecycle management ... (LCM) programs. This role contributes to regulatory dossiers across US, EU, and other regions (eg,...cGMP requirements and small-molecule products; experience with aseptic or medical device products is a plus. + Proficiency in… more
- System One (Bellevue, WA)
- Job Title: Nuclear Plant Program Specialist and Procedure Writer Location: Bellevue, WA Type: Contract Contractor Work Model: Remote Position Overview: As a ... Nuclear Plant Program Specialist and Procedure Writer , you will play a pivotal role in the...approaches to administrative and operational procedure development. + Implement regulatory review processes in accordance with standards like 10CFR50.59… more
- System One (Bellevue, WA)
- Job Title: Chemistry Specialist and Procedure Writer Location: Bellevue, WA Type: Contract Compensation: $84 - $135 hourly Contractor Work Model: Remote Key ... processes, leveraging smart procedures and other software-based tools. + Regulatory Compliance: Execute essential reviews under 10CFR50 and 10CFR72.48, ensuring… more
- Noblis (Washington, DC)
- Responsibilities **Overview** We are seeking an experienced **Senior Technical Writer /Editor** with a deep understanding of aviation operations, flight procedures, ... NAS operations, and flight procedures** to ensure technical accuracy and regulatory alignment. + Analyze existing and potential content to identify opportunities… more
- CH Robinson (Eden Prairie, MN)
- …the world's largest logistics platforms and we're looking for our next **Customs Entry Writer ** . Is that you? You'll be responsible for the accurate and timely ... expert in our systems and processes and provide on-going regulatory training. Many of our successful Customs Entry Writers...creativity and driving impactful results. With the flexibility for remote work two days a week, this role strikes… more
- Collins Aerospace (PR)
- …offered. This role is categorized as hybrid, with 3 days onsite and 2 days remote following the schedule assigned by the Manager. What YOU will do: + Conduct ... to ensure quality, cost-efficiency, and compliance with customer and regulatory requirements. + Review and analyze engineering drawings, schematics, software… more
- RTX Corporation (Aguadilla, PR)
- …This role is categorized as **hybrid** , with 3 days onsite and 2 days remote following the schedule assigned by the Manager. **What YOU will do:** + Conduct ... to ensure quality, cost-efficiency, and compliance with customer and regulatory requirements. + Review and analyze engineering drawings, schematics, software… more
- Stantec (Sacramento, CA)
- …Region (serving Northern California and parts of Nevada) is seeking a Senior Regulatory Waters Permitting Specialist with at least 10 years of experience leading and ... a hybrid model (ie, a combination of office and remote working) and robust benefits package. As a Senior... working) and robust benefits package. As a Senior Regulatory Waters Permitting Specialist, you will provide preparation, negotiation,… more
- Coinbase (Charlotte, NC)
- …you, there's no better place to be. While many roles at Coinbase are remote -first, we are not remote -only. In-person participation is required throughout the ... GRC teams, Legal and Compliance for risks, assessments, and reporting to meet regulatory requirements. * Support audit and regulatory inspections: Support data… more
- Merck (Durham, NC)
- …product disposition + Preparing and/or providing guidance and review for regulatory filings, process descriptions, investigations, and change requests. Acts as a ... participant in domestic and international regulatory agency inspections + Supporting all quality and safety initiatives + Provide technical support to manufacturing… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- **Job Description Summary** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our Purpose, and it's no ... Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our… more
- IQVIA (Durham, NC)
- …teams that include Project Manager, CRA, Data Manager, Biostatistician, Programmer, and/or Medical Writer . + Maintain awareness of overall developments in the ... dedicated to reshaping the future of healthcare. **Additional Benefits:** + Home-based, remote work opportunities. + Work/life balance. + Collaborate on projects and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …timely cleaning and delivery of clinical trial data. Coordinates and supports Trial Medical Writer in providing the CTR. + Responsible for timely, complete, ... documents owned by other functions (eg, Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring). + Verifies and provides input into the… more
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