Remote Lead Nonclinical Writer - Regulatory Submissions
MMS
- Remote job
A leading clinical research organization is seeking a nonclinical regulatory writer to join their remote team. You will develop and manage comprehensive nonclinical documents while ensuring compliance with regulatory guidelines. Candidates should hold a BS in pharmacology or related field, with 2+ years of relevant experience. The role requires strong analytical skills and the ability to collaborate within a supportive team. This is a unique opportunity to drive contributions in a highly respected organization known for its exceptional culture. #J-18808-Ljbffr MMS
- ...A clinical research organization is seeking a Regulatory Writer to manage and develop technical nonclinical documents. This full-time, remote position requires at least 2 years of writing experience in the pharmaceutical industry, strong analytical skills, and proficiency...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 various... ...strong writing skills, regulatory knowledge, and the ability to...Remote workRegulatoryFull time
$80 - $90 per hour
Eightelevengroup is looking for a Lead Medical Writer based in Eastern Standard Time (EST) for a 2-month remote contract. The role involves autonomously... ...writing and reviewing clinical regulatory documents, contributing to submission teams, and mentoring junior writers...Remote jobRegulatoryHourly payContract work$130k - $150k
Praxis Precision Medicines, Inc. is seeking a talented Medical Writer to oversee documents for clinical development programs. This role... ...’s degree in a scientific discipline. Responsibilities include leading the preparation of clinical trial documents and collaborating...Remote jobRegulatoryFlexible hours- ...approach to complex trial data and regulatory submission challenges. With a global... ...not only maintains an industry-leading customer satisfaction rating but... ...management of highly technical nonclinical documents. This is a full-time, remote position. Roles and Responsibilities...Remote workRegulatoryFull time
- ...A leading life sciences company is seeking a Regulatory Operations Manager to oversee the publishing of deliverables for electronic submissions to health authorities. The role involves vendor oversight... ...the US and Europe. This is a remote position requiring expertise in...Remote workRegulatory
- A biopharmaceutical company seeks a Regulatory Medical Writer in Los Angeles, CA. This role involves preparing, reviewing, and editing regulatory documents for submission to the FDA, ensuring compliance with guidelines. Required qualifications include a Bachelor’s degree...Regulatory
- A leading staffing firm is seeking a Medical Author to document clinical data and regulatory submissions to support drug development. This role requires expertise in analytical writing, project management, and collaboration with product teams to ensure high-quality deliverables...Regulatory
$160k - $175k
...cancer and beyond. Our lead program, palazestrant... ...> Lead Senior Medical Writer As the Lead Senior Medical... ...scientific and regulatory documents supporting Olema... ...for regulatory submissions, medical communications... ...Experience working in hybrid/remote environments...Remote workRegulatoryWork at officeFlexible hours- ...Praxis Precision Medicines, Inc. is searching for a Senior Regulatory Submissions Manager to oversee regulatory submissions to U.S. and international... ...match, stock incentives, and generous PTO. This position offers a remote work option with travel as needed. #J-18808-Ljbffr...Remote workRegulatory
$128k - $156k
Disc Medicine in Watertown, MA, is seeking a Regulatory Operations Manager to manage regulatory submissions and document compliance activities. This full-time role requires 5-7 years of direct experience and expertise in MS Word and Veeva RIM. Responsibilities include...Remote jobRegulatoryFull time- ...biotechnology company is seeking a Senior Specialist for Regulatory Operations to manage regulatory submissions and support systems in Frederick, MD. This role... ...submission standards. Responsibilities include leading submissions, working with vendors, and overseeing document...Remote jobRegulatory
$130k - $160k
A leading diagnostics firm is seeking a Manager, Medical Writing,... ...team and ensuring high-quality regulatory documents for market submissions. The role includes mentoring writers, managing deadlines, and... ...sector. The position is fully remote, offering a compensation range...Remote jobRegulatory$70k - $130k
...company is seeking a Senior Specialist in Regulatory Operations to manage regulatory submissions across their development pipeline. The role involves leading submission management and ensuring... ...field. The position can be remote or based at the company's office in...Remote jobRegulatoryWork at office- ...Proposal Writer Senior Lead As a global leader in micromobility, Lime is on a mission to build... ...and key messaging for public sector regulatory audiences about our programs, technology... ...written documents. This is a remote position with a requirement for candidates...Remote workRegulatoryLocal area
$130k - $150k
...biopharmaceutical firm is seeking a Medical Writer to support clinical development programs... ...responsible for producing high-quality regulatory documents and collaborating with cross-... ...of $130,000 - $150,000 USD annually, remote work flexibility, and a comprehensive benefits...Remote workRegulatory$300k - $330k
...seeking an experienced VP of Nonclinical Development to execute non-... .... Responsibilities include leading non-clinical strategies,... ...toxicology studies, and preparing regulatory submissions. The position offers a... ...benefits, and a remote work option. #J-18808-Ljbffr...Remote workRegulatory$50k - $75k
...Customs Entry Writer - On-site Springfield, NJ Salary: $50,0... ...experience and qualifications) Remote Option: No About Us... ...coordination and entry summary submissions Maintain clear communication... ...skills to navigate complex regulatory environments. Benefits...Remote workRegulatoryWork at office- ...Therapeutics, Inc in Boston is searching for a Toxicology Lead to guide nonclinical safety and toxicology work for drug candidates. The... ...collaborating with research and development teams, and handling regulatory submissions. The ideal candidate should possess a PhD or DVM with...Regulatory
- Regulatory & Medical Affairs - Nonclinical Regulatory Document and Scientific Writer EEO: "Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."Regulatory
- ...Barrington James is seeking a Regulatory Affairs CMC Specialist/Manager to lead client regulatory CMC projects. This fully remote role requires 7+ years of regulatory affairs experience... ...expertise, and proficiency in managing submissions for INDs and NDAs. The successful...Remote workRegulatory
$60 - $65.21 per hour
...Job Title: Lead R&D Technical Writer Location: Portage, MI Type: Contract... ...0-65.21/hr Work Model: Remote – offsite Be part... ...and support clinical and regulatory documentation efforts, influence... ...to deliver high-quality submissions on schedule. Ideal...Remote workRegulatoryContract workWork experience placementLocal area- ...A leading healthcare company is seeking a Manager of Regulatory Affairs based in remote locations. You will develop and execute regulatory strategies, manage FDA submissions, and ensure compliance for innovative medical devices. The ideal candidate has over 8 years of...Remote workRegulatoryFull time
- Curium Pharma is seeking a (Contractor) Regulatory Affairs Technical Writer in St. Louis, MO. This role involves coordinating regulatory activities and submission content to support key projects. Candidates should have at least a Bachelor's Degree in a technical discipline...RegulatoryContract workFor contractors
- ...Job Title: Scientific Writer (Non-Clinical) Location: Irvine, CA (Hybrid: Tuesday–Thursday Onsite / Monday & Friday Remote) Duration: 6 Months (Backfill) Role Overview... ...reports, journal manuscripts, and regulatory submission modules. The ideal candidate thrives...Remote workRegulatoryLocal areaMonday to FridayShift work
- ...A leading life sciences company is seeking a Senior Regulatory Affairs Manager to lead their dynamic team through global clinical trials. The role involves driving submission planning, ensuring compliance with regulatory authorities, and managing multiple priorities....Remote workRegulatory
$115k - $185k
...A medical device company is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and strategy for new product development. This role offers flexibility in levels and can be remote, aligned with US East Coast hours. Candidates should have a Bachelor...Remote workRegulatory- Regulatory Writer Opportunity Our client, located in Chapel Hill, NC, is a professional services... ...review, and electronic regulatory submissions for pharmaceutical, biotech, and medical... ...supported global clients with a fully remote team of scientifically trained professionals...Remote workRegulatory
- ...biotechnology consulting firm is seeking a Regulatory Affairs Consultant to support... ...10-20 hours of work per week. This remote position requires expertise in regulatory... ...products. Responsibilities include leading regulatory submissions, engaging with the FDA, and...Remote workRegulatory10 hours per week
- ...scientific approach to complex trial data and regulatory submission challenges. With a global footprint... ...Under minimal supervision, the Medical Writer will critically evaluate, analyze, and... ...clinical study protocol experience, as lead author, required Experience leading...Remote jobRegulatoryWorldwide
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Lead Nonclinical Writer - Regulatory Submissions. Be the first to apply!


