Remote Medical Writer for Phase I/II Clinical Reports
Celerion
- 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
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...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 area- Medical Writer II job at US Tech Solutions. Remote. Location: Remote. Duration: 12 months contract. Job Description Defines scope of quality control activities... ...business processes. Maintain strong knowledge of clinical regulatory documents requiring quality control...Remote jobContract work
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...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 area$35.38 - $44 per hour
...Medical Writer IIEastridge Workforce Solutions is committed to connecting skilled professionals... .... We are seeking a Medical Writer II to support our client's team. The hourly... ...: Aliso Viejo, CA.Job Summary:Prepare clinical study reports (CSRs) by translating data tables,...Hourly payTemporary workWork at officeMonday to Friday- ...to pharmaceutical companies, medical device companies, biotech organizations... ...staffing needs across clinical research, pharmacovigilance,... .... Job Title: Medical Writer II Job Location: Aliso Viejo,... ...: Prepare clinical study reports (CSRs) under supervisor direction...Contract workWork experience placementWork at office
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- 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
- ...Remote Medical Writer Required Skills & Experience: Bachelor's degree in a... ...protocol development, writing clinical section for regulatory... ...submission and clinical evaluation report writing; Ability to identify... ...Class III), IDE (US Class II/III), 510K (US Class III), other...Remote work
- ...Clinical Research Coordinator IIThe Clinical Research Coordinator II handles administrative activities generally associated with the... ...source documents/case report forms.Provides guidance to less... ...an Emory University location. Remote work from home day options may...Remote workWork from home
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- ...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
- ...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
- Moffitt Cancer Center is seeking a Protocol Writer I to support investigator-initiated, early-phase clinical trials. You will write, edit, and complete clinical trial protocols and related documents for timely SRC submissions, under the direction of the Principal Investigator...Work at office
$90 - $150 per hour
...Role Overview Contribute to clinical data and reporting workflows by generating and validating high-quality... .... Experience with pre-market Phase 1, 2, and 3 clinical trial data and clinical... ...-horizon authorship. Work Terms Remote, hourly engagement. Availability of...Remote workHourly pay$82.93k - $126.43k
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