Remote Medical Writer for Phase I/II Clinical Reports
Celerion
New York, NY
- Remote job
Celerion is seeking a Medical Writer to work remotely. The role analyzes and interprets safety results from clinical trials, compiling, writing and editing clinical study reports and other industry documents. It requires accurate classification of events and medications using standardized coding systems. Responsibilities include drafting phase I/II documents, QC of safety text, and leading multi-disciplinary scientific reports while ensuring compliance with GCP/ICH and client specifications. #J-18808-Ljbffr Celerion
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Remote Medical Writer for Phase I/II Clinical Reports in New York, NY vacancy
$105k - $118k
...Our Phase I team is currently seeking a Clinical Research Associate II with 1+ years of on-site monitoring experience. Ideal candidates... ...of the data submitted on Case Report Forms (CRFs) or other data... ...Range: $105 - $118K #LI - Remote Applications will be accepted...Remote workWork at officeLocal areaNight shift$50 - $80 per hour
...Overview Apply regulatory medical writing expertise to author and evaluate clinical documentation used to... ...from Clinical Study Reports, Development Safety Update... ...multiple clinical phases and therapeutic areas;... ...Contractor. Location: Remote. Project focus: Contributing...Remote workHourly payFor contractorsSaidGig
United Statesa month ago$100k - $120k
...Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates... ...integrity of the data submitted on Case Report Forms (CRFs) or other data... ...Target Pay Range: $100 - $120K #LI - Remote Applications will be accepted on...Remote workWork at officeLocal areaNight shift$125k - $160k
...Clinical Documentation Improvement Specialist II When you join the growing BILH team, you're... ...lives. **This position is remote. Candidates must be... ...providers as supported by medical record documentation to... ...used for measuring and reporting physician and hospital quality...Remote workWork at officeLocal areaBeth Israel Lahey Health
United States5 days ago- MMS Holdings Inc is seeking a skilled Medical Writer in Chicago. The successful candidate will have a strong background in regulatory writing, including clinical protocols and study reports. They will ensure quality documentation while mentoring fellow team members and...Remote job
- Syneos Health, Inc. is seeking a Sponsor Dedicated Protocol Medical Writer II/Sr for a remote-based role. You will lead the creation and review of... ...sites with mentorship to junior writers. You will work with clinical scientists, data management, and regulatory staff to...Remote job
$50 - $80 per hour
...Overview Apply regulatory medical writing expertise to author and evaluate clinical documentation that... ...submissions and safety reporting. Key Responsibilities... ...across multiple clinical phases and therapeutic areas,... ...type, contractor, remote work. Work is performed...Remote workHourly payContract workFor contractorsLocal areaSaidGig
United States6 days ago- ...to pharmaceutical companies, medical device companies, biotech organizations... ...staffing needs across clinical research, pharmacovigilance,... .... Job Title: Medical Writer II Job Location: Aliso Viejo,... ...Responsibilities: Prepare clinical study reports (CSRs) under supervisor...Contract workWork experience placementWork at office
HonorVet Technologies
Aliso Viejo, CA4 days ago $50 - $80 per hour
...Job Description Job Description Job Title: Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50–$80/hour Job... ...Responsibilities Author and review Clinical Study Reports (CSRs) and other regulatory documents....Remote jobFor contractorsYO AI Labs
Houston, TX17 days ago$35.38 - $44 per hour
...professionals with meaningful career opportunities. We are seeking a Medical Writer II to support our client's team. Created/Revised Date: 08... ...0 AM-5:00 PM (100% Onsite) Job Summary: Prepare clinical study reports (CSRs) by translating data tables, listings, and figures...Hourly payTemporary workWork at officeLocal areaMonday to FridayEastridge Workforce Solutions
Aliso Viejo, CA3 days ago- ...sites participating in early phase oncology clinical research trials, the full-... ...Clinical Research Site Liaison II will ensure compliance with... ..., and data collection in a remote environment. Key responsibilities... ...enrollment, safety event reporting, and data collection...Remote workFull time
Virtual Vocations Inc
United States2 days ago - Medical Writer (Consultant) - Clinical Development / Early Feasibility Study Contract-6-12+Months Seattle, WA- Remote Immediate Need Candidates residing in Europe are also encouraged to... ...progresses through FDA review and clinical phases, with potential for long-term...Remote workContract workImmediate start
- Medical Writer II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster... ...of clinical data (e.g., from clinical study reports, safety summaries, biostatistical tables,...
- Resourcing Life Science is seeking a Senior Clinical Research Associate (CRA) to work from home in Florida. In this role, you will monitor clinical studies in phases II-III, ensuring adherence to Good Clinical Practices and supervising study conduct according to required...Remote jobWork from home
- ...Senior Medical Writer, Publications (Remote, US) Location: Remote (US-based) Schedule: Full... ...of high-impact clinical publications and scientific... ...-on experience developing Phase III clinical trial manuscripts... ...protocols, clinical study reports, statistical outputs, and...Remote workFull time
EPM Scientific
New York, NY5 days ago - ...Title: Sr. Medical Writer BIOMARIN REMOTE Can work EST or PST Hours Strong... ...industry, with expertise in clinical study documentation,... ...documents used in conducting and reporting the results of clinical... ...documentation in all phases of drug development. Medical...Remote workFull timeFor contractorsWork at officeShift work
3B Staffing LLC
New York, NY5 days ago - ...Medical Writing Specialist For the past... ...regulatory sciences, clinical research solutions... ...) across all phases of clinical research... ...amendments, study reports, patient narratives... ...experienced medical writers, as necessary.... ...ProPharma supports remote working, we also recognize...Remote workContract workWork at office
ProPharma Group
Chicago, IL1 day ago - ...Provides high-quality regulatory medical and scientific writing in support of Phase 1-3 clinical development of pharmaceutical... ...amendments, and Clinical Study Reports (CSRs). Researches, authors... ...documents prepared by junior writers and peers. May provide training...Remote workContract work
Katalyst Healthcares and Life Sciences
United States1 day ago - ...Objective Reporting to the Head of Medical/Regulatory Writing, the Medical Writer – Clinical Regulatory Documentation will be responsible for the preparation and delivery... ...of clinical development, including early-phase studies, late-stage clinical trials, and...Full timeLocal area
Perspective Therapeutics
United Statesmore than 2 months ago - Clinical Studies Engineer IIBIOTRONIK is one... ...distribute high-quality medical products based on... ...Studies Engineer II to join our... ...analysis, clinical reporting, and regulatory submissions... ...in all phases of clinical investigations... ...campus -or- remote within the United...Remote workFull timeContract work
- ...Clinical Research Associate II Precision for Medicine is not your typical CRO. We... ...are conducted, recorded, and reported per protocol, SOPs, ICH-GCP... ...healthcare discipline Phase I experience Experience... ...industry-leading operational and medical experts, advanced biomarker...Remote workLocal areaNight shift
Precision for Medicine
United States5 days ago - ...role focuses on translating brand strategy, clinical data, and approved claims into engaging... ...or compliance. Skills: Fully remote, possibility to extend, no specific degree... ...regulated landscape, familiarity with MLR (medical legal and regulatory process) Education...Remote work
SGS Consulting
Remotemore than 2 months ago - SGS in Richardson, TX is seeking a technical writer to draft protocols and reports for clinical studies on cosmetics or other claims, ensuring alignment with ICH and GCP guidelines. You will coordinate internal and external protocol reviews, maintain templates and SOPs...
- Emerald Clinical Trials Emerald Clinical Trials is a global... ...solutions across all phases, offering Phase I-IV... ...Clinical has helped drive medical breakthroughs through... ...including clinical study reports, clinical study... ...Flexibility: Enjoy hybrid or remote working arrangements, depending...Remote workLocal areaWorldwide
- ...our academic community.DescriptionThe Clinical Research Coordinator II handles administrative activities... ...and completes source documents/case report forms.Provides guidance to less experienced... ...at an Emory University location. Remote work from home day options may be granted...Remote workWork from home
- Opportunity Details On Assignment Medical Writer Remote USA The primary... ...control review of submission reporting documents in accordance with... ...MW will: collaborate with clinical study teams, doctors, scientists... ...deliverables covering all phases of clinical research for...Remote workWork experience placement
- Medical Writer - Oncology Clinical Trials Location: Remote or Hybrid in Waltham, Massachusetts preferred. Candidates must be... ...and amendments Clinical study reports (CSRs) Clinical sections of INDs... ...Experience in authoring documents for Phase I-III oncology trials and...Remote workFor contractorsFlexible hours
- ...our portfolio of late clinical-stage products that address... ...at Telix The Medical Writer will contribute to the... ...documents necessary for all phases of clinical drug... ...BLAs), clinical study reports, clinical study protocol... ...medicine. We have hybrid and remote employees located all...Remote work
- ...Clinical Trial Investigator Serve as main CTI contact... ...Manager. Conduct remote monitoring and complete... ...Plan. Utilize systems and reports to track subject status... ...pharmaceutical, biotechnology, and medical device firms. For more... ...to move onto the next phase of our hiring process,...Remote workContract workInterim roleWork from home
CTI
United States1 day ago $60 - $65 per hour
...learn more. Base pay range $60.00/hr - $65.00/hr Immediate need for a talented Medical Writer II . This is a 12+months contract opportunity with long-term potential and is located in U.S (Remote) . Please review the job description below and contact me ASAP if you are...Remote workContract workPart timeLocal areaImmediate start
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Medical Writer for Phase I/II Clinical Reports. Be the first to apply!
Related searches
- medical writer New York, NY
- medical writer remote New York, NY
- senior medical writer New York, NY
- medical editor New York, NY
- supply chain analyst remote New York, NY
- procurement specialist remote New York, NY
- physician consultant remote New York, NY
- remote insurance agent New York, NY
- remote data manager New York, NY
- training manager remote New York, NY