- Chickasaw Nation Industries, Inc. (CNI) (Rockville, MD)
- The Technical Writer - Training Development provides support to the agency by developing and fully executing new Standard Operating Procedures (SOP's). This position ... and online learning modules. This full-time position is currently remote to the Rockville, MD area; however, it might...the first day of hire to full time employees; ( Medical - Dental - Vision), Company Life Insurance, Short-Term… more
- Solomon Page (North Chicago, IL)
- We are currently hiring multiple experienced Principal Medical Writers to support regulatory writing efforts across all phases of clinical development (Phase ... I-IV) and therapeutic areas. These are remote contract opportunities with flexible hours, ideal for professionals seeking ad hoc, part-time, or full-time… more
- Battelle (Columbus, OH)
- …substances and evaluate their effects on human health. The technical report writer and study director will support scientific research that safeguards public health, ... all required training. Follows FDA GLP and other appropriate regulatory (eg, OECD, ICH) requirements to ensure all experimental...model allows you to work 60% in-office and 40% remote , with Monday and Tuesday as common in-office days,… more
- ThermoFisher Scientific (Greenville, NC)
- …Service Partnership (FSP) Team and are seeking candidates based in the US! As a remote -based Senior Medical Writer within the FSP team, you will provide ... high-quality medical and scientific writing from planning and coordination through...possess the versatility to author both clinical and preclinical regulatory documents, with therapeutic area expertise in infectious diseases… more
- Actalent (Philadelphia, PA)
- Lead Medical Writer Job Description We are seeking a highly experienced Senior Medical Writer to join our team and contribute significantly to our ... 10+ years of medical writing experience. + Experience with clinical and regulatory documents. + Experience working with a sponsor, preferably in small pharma. +… more
- Medtronic (AL)
- …to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. ... its intended purpose. + Create & maintain plans and reports for regulatory authorities. + Review/approve other documentation for device development. + Knowledge of… more
- System One (Cleveland, OH)
- …annually Contractor Work Model: Remote As a Director or Senior Director, Medical Writer you will be responsible for document creation across clinical ... Job Title: Director / Senior Director Medical Writer Location: CST or EST... documents, reports and protocols through implementation of the regulatory medical writing process in collaboration with… more
- BeOne Medicines (Emeryville, CA)
- **General** **Description:** We are seeking a highly experienced and strategically minded Medical Writer to lead the tactical execution of publications stemming ... phase development to marketed products. In this role, the Medical Writer will serve as a key...research in the oncology space + Familiarity with global regulatory and medical affairs environments (eg, US,… more
- J&J Family of Companies (West Chester, PA)
- …of America **Job Description:** We are searching for the best talent for a **Senior Medical Writer , Scientific Operations,** to join our MedTech Team. Remote ... journey to wellness. Learn more at https://www.jnj.com/medtech **Purpose:** The Senior Medical Writer , Scientific Operations provides oversite and execution of… more
- System One (Spring, TX)
- Job Title: Technical Writer Location: Spring, Texas Type: Contract To Hire Compensation: $35 - $50 hourly Contractor Work Model: M/F from home T/W/Th in office Job ... Title: Technical Writer Job Summary: We are seeking a detail-oriented and...Experience with document management systems. + Knowledge of industry regulatory requirements and standards. + Certification in technical writing… more
- Dairyland Power Cooperative (La Crosse, WI)
- …work experience, growth and professional development. **Work Methods Coordinator/Technical Writer -Safety (Hybrid - La Crosse, WI)** **Hiring Salary Range: $99,900 ... process changes or introduce latest items. 6. Prepare the organization for regulatory changes that will require changing process or tooling; collaborate with Safety,… more
- Actalent (Minneapolis, MN)
- …Adobe Photoshop, and document management systems is a plus. + Knowledge of regulatory affairs and medical device labeling. + Graphic design and editing ... home in the morning and attending afternoon meetings in the office. Remote work is possible during adverse weather conditions. Responsibilities + Create, revise,… more
- J&J Family of Companies (Spring House, PA)
- …by the Company. **We are searching for the best talent for Associate Director, Regulatory Medical Writing - Oncology.** **Purpose:** + Able to function as a ... be a hybrid (3 days in office and 2 remote ) OR Remote role available in all...is required. + At least 8 years of relevant clinical/ regulatory medical writing experience is required. +… more
- Clay Lacy Aviation (Van Nuys, CA)
- …reviews, data governance, security strategy and compliance audits. + Location: Remote + Compensation: $88,000 - $140,000 per year. This position includes ... comprehensive medical , dental, and vision benefits. Duties and Responsibilities System...analytical reports with business and analytics leaders, using report writer and calculated fields to support strategy, planning and… more
- Lineage Logistics (Tacoma, WA)
- Additional Job Description ** Remote Customs Entry Writer ** **Schedule:** Monday-Friday | 8:00 AM - 5:00 PM **Location:** Remote (Equipment Provided) We are ... seeking a detail-oriented and experienced **Customs Entry Writer ** to join our team. In this critical role,...customs officials, clients, and transportation partners. This is a ** remote position** , and all necessary equipment will be… more
- System One (Tarrytown, NY)
- …Writing Specialist Type: Contract Compensation: $55 - $57 hourly Contractor Work Model: Remote Hours: 8 AM- 5 PM M-F Responsibilities: Help with drafting and ... + Abide by and keep current with GxP and regulatory guidelines and all company SOPs or working practices...science background/education with 5-7 years experience + Non clinical writer for reg submission documents, non clinical pharmacology +… more
- Battelle Memorial Institute (Columbus, OH)
- …substances and evaluate their effects on human health. The technical report writer and study director will support scientific research that safeguards public health, ... required training. + Follows FDA GLP and other appropriate regulatory (eg, OECD, ICH) requirements to ensure all experimental...model allows you to work 60% in-office and 40% remote , with Monday and Tuesday as common in-office days,… more
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