Remote Clinical Research Source Writer - QA/Regulatory
Arizona Liver Health
A leading health research institute is seeking an experienced Source Writer with QA/QC/Regulatory expertise. You will ensure high standards of scientific excellence while contributing to transformative liver health initiatives. Responsibilities include generating source documents, performing QA reviews, and ensuring compliance with clinical research regulations. The ideal candidate will have a relevant degree and experience in clinical research. Competitive salary and benefits offered including health insurance, 401K match, and educational assistance. #J-18808-Ljbffr
$50k - $70k
...innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and... ..., multitherapeutic research, standard of care,... ...seeking an experienced Source Writer with a background in QA/QC/Regulatory. As a... ...AZ, Tucson, AZ, or Remote-US in preferred locations...Remote workRegulatoryFull timeTemporary workLocal area- ...MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves... ...scientific approach to complex trial data and regulatory submission challenges. With a global... ...to author based on highly technical sources such as GLP and non-GLP nonclinical...Remote workRegulatory
- Remote Jobs is seeking a Quality Specialist to ensure accuracy... ..., and compliance of source document templates for multiple clinical trial sites. You will... ...CRIO, data management, and regulatory staff to maintain... ...have 2+ years in clinical research with CFR/GCP/HIPAA knowledge...Remote workRegulatory
- ...Job Title: Copywriter/QA Content Specialist (Legal... ...Team) Location: Remote Duration: 12 Months to... ...ongoing compliance and regulatory awareness efforts. Your... ...Specialist or Content Writer, or in a related role,... ...partnering with designers and sourcing appropriate images to enhance...Remote workRegulatory
- A leading clinical research organization is seeking a technical writer to develop and manage nonclinical documents. This full-time remote position requires a BS in pharmacology or related fields... ..., with a minimum of 2 years in regulatory writing. Candidates should...Remote workRegulatoryFull time
- A leading clinical research organization is seeking a Nonclinical Writer to develop and manage highly technical nonclinical documents. This remote, full-time role involves close collaboration with... ...requires strong writing skills, regulatory knowledge, and the ability to...Remote workRegulatoryFull time
$70k - $85k
A clinical research organization is seeking an entry-level regulatory writer to join their innovative team in Seattle. This full-time, remote position involves developing and managing nonclinical documents while collaborating with cross-functional teams. Candidates should...Remote jobRegulatoryFull time- ...scientific documents related to clinical trials, the full-time Senior Medical... ..., collaborate with medical writers, and mentor junior staff in a remote work environment. Key responsibilities... ...understanding of clinical research and regulatory documentation Exceptional editing...Remote workRegulatoryFull time
- ...Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to... ...responsible for leading the development of high-quality regulatory and clinical documents that effectively...Remote workRegulatory
$85k - $100k
...prove it! The Medical Writer plays a critical role... ...'ll translate complex clinical data into clear,... ...meets client objectives, regulatory requirements, and the... ...clinical trial results, research studies, and other scientific... ...#LI-Remote MJH Life Sciences provides...Remote workRegulatoryTemporary workWork at office- ...involves contributing to clinical research, developing innovative... ...and brachytherapy sources, to ensure accurate dose... ...such as the Nuclear Regulatory Commission (NRC), Food... ...Quality Assurance (QA): Conducting regular quality... ...Yes, 10 % of the Time Remote Work: No Job Posting:...Remote workRegulatoryFull timeWork experience placementLocal area
- ...Sr. Medical Writer Integrated Resources, Inc is a premier staffing... ...Technology (IT), Clinical Research, Rehabilitation Therapy and... ...Scientific Communications group. Remote candidates are an option.... ...writing, editing and reviewing regulatory (e.g. Clinical Evaluation...Remote workRegulatoryWork at officeLocal areaRelocation
- ...lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance,... ...mentors less experienced medical writers, as necessary. ~ Adheres to established... ...not. Whilst ProPharma supports remote working, we also recognise the value...Remote workRegulatoryContract workWork at office
- ...Job Description POSITION TITLE: Regulatory Writer I DEPARTMENT: Regulatory Ora Values... ...building the future of ophthalmic clinical research. As the world's leading full-service... ...you and your family feel secure. Remote & Wellness Reimbursement: We'll reimburse...Remote workRegulatoryDaily paidFull timeWork experience placementFlexible hours
- ...Medical Writer (Consultant) – Clinical Development / Early Feasibility Study Contract... ...12+Months Seattle, WA- Remote Immediate Need... ...internal SMEs, who will provide source materials, guidance, and... ...Ensure alignment with regulatory expectations and submission...Remote workRegulatoryContract workImmediate start
$105k - $125k
...Senior Regulatory Medical Writer (FSP; Remote; US) At Thermo Fisher Scientific, you will discover meaningful work... ...taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and...Remote workRegulatoryTemporary workLocal areaFlexible hours- A leading global clinical research organization is seeking a Senior Medical Writer I for a 12-month FTC, fully remote. In this role, you will spearhead the development and execution... ...possess exceptional communication and regulatory knowledge. Competitive salary and...Remote jobRegulatoryFixed term contract
- ...Specifications Writer Award-Winning 50-person distinguished architectural practice is actively seeking a Specifications Writer to... ...demonstrated expertise in the International Building Code (IBC) and regulatory requirements specific to California jurisdictions Technology...Remote workRegulatoryFull timeLocal area
- ...Working remotely on a contract basis, the Technical Report Writer will draft and edit technical reports, meeting summaries... ...technical reports based on existing source materials Transform technical... ...writing technical reports, regulatory documents, or similar materials...Remote workRegulatoryContract work
$33 - $35 per hour
...experienced AML SAR Writer "This role is currently... ...android or iphone for remote access into the client... ...are generated from sources which include... ...searches etc.) • Conduct research over available Bank systems... ...with applicable regulatory requirements preferred...Remote workRegulatoryContract workWork at officeImmediate start- ...drug safety, health economics and outcomes research, regulatory affairs, quality assurance, compliance and... ...Job Description My Client is in need of a Clinical Narrative Writer. The position is a 3 month, 40 hour a week REMOTE engagement. The therapeutic areas include Cardiology...Remote workRegulatory
- ...the development of high-quality clinical study documents, the remote Senior Medical Writer will manage clinical document... ...while ensuring compliance with regulatory guidelines. Key responsibilities... ...teams Conduct literature-based research to support writing activities...Remote workRegulatory
- ...Regulatory Writer and/or Regulatory QC/ Editor Remote - United States Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to... ...consistency of documents versus their source materials Define and confirm the scope...Remote workRegulatoryTemporary work
- ...and independently in hybrid or remote work environments. • You... ...effectiveness and alignment with regulatory requirements. 4. Evaluates... .... 6. Plans, conducts research, and develops operational reference... ..., and other defined sources; drafts, formats, edits, and...Remote workRegulatoryWork experience placementFlexible hoursAfternoon shiftEarly shift
- ...scientific meetings. Adheres to established regulatory standards, including but not limited to... ...quality and editorial reviews. Ensures source documentation is managed appropriately.... ...and leads less experienced medical writers on complex projects, as necessary. Develops...Remote workRegulatoryFlexible hours
- ...scientific approach to complex trial data and regulatory submission challenges. With a global... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and... ...rigor and absence of bias Write and edit clinical development documents, including but not...Remote workRegulatoryWorldwide
$100k - $160k
...Market Access Medical Writer New York, New... ...access strategy. Remote position (EST... ...translate complex clinical data into clear, compelling... ...compliant with regulatory guidelines.... ...Identify credible sources and ensure adherence... ...medical messaging. Research, Thought...Remote workRegulatoryFlexible hours$115k - $140k
...Reporting Mode: 100% remote from anywhere in the United... ...-oriented Epic Report Writer to architect solutions... ...Epic, supporting clinical, operational, and financial... ...validation against source systems Troubleshoot... ...response to workflow, regulatory, or system changes Provide...Remote workRegulatoryPermanent employmentFull timeMonday to Friday$55.3k - $126k
...Technical Writer Write and edit technical and program documentation... ...matter experts and analyze source materials to translate... ...control. Apply relevant quality, regulatory standards, and best practices... ...cameras on during meetings. Remote: If this position is listed...Remote workRegulatoryFull timeContract workPart timeWork at officeLocal area$62k - $108.6k
...Sr. Medical Editor (Regulatory Documents + QC) - US Home Based Syneos... ...and accelerate progress. Our Clinical Solutions team members act... ...data in documents against the source tables, figures, and listings... ...and updates the lead medical writer, project manager, and/or...Remote workRegulatoryWork from homeFlexible hours
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