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Thus, the candidate should also have an understanding of various clinical trial activities such as Clinical Trial Management Services, clinical monitoring, data management, Real World Data/Evidence (RWD/RWE), biostatistics, medical writing, Ph 1 CRU, central lab, biomarker lab, bioanalytical lab, RTSM, eCOA, medical imaging, safety, e-informed consent, mobile HCP services, telemedicine and wearables/sensors.
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The individual in this role will be the analytical, technical, and quality operational subject matter expert (SME) for QC CMC writing, review and assist in Regulatory filings (ICH/Compendial/FDA and EMA.
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Demonstrate clear verbal and written communication and listening skills, both in person and on the phone, using spoken and written English; bilingual English/Spanish speaking and writing skills preferred.
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Trial Master File (eTMF) The role also involves coaching VO team members to resolve issues from a QC standpoint and serving as a primary reviewer of QC data for inspection readiness. and Contract Repositories to ensure meticulous oversight of VOs documentation, adherence to work procedures, compliance standards, and the preservation of data integrity.
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Must be fluent in reading, writing, and speaking English. Basic Qualifications One year of prior leadership, supervisory, or retail key holder work experience. Except in Puerto Rico) Preferred Qualifications Prefer the knowledge of store inventory control.
$18 - $20 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Deep learning expertise: Experience training deep-learning models in an end-to-end fashion, writing custom layers/operations, optimizing networks for inference on embedded systems. You are passionate about ML, both large scale engineering and research challenges, especially in the space of autonomous driving and/or robotics.
$180,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Oversee recruitment and manage medical writers and contractors to ensure the highest quality of medical writing and adherence to Gilead document standards. Optimize medical writing processes and templates for protocols and ensure adherence to Gilead documentation standards.
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Daily activities will include, but are not limited to, working within a team environment and leading functional internal audits of VOs electronical Trial Master File (eTMF) and Contract Repositories to ensure meticulous oversight of VOs documentations, adherence to work procedures, compliance standards, and the preservation of data integrity.
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Content Marketing is looking for a content and editorial intern with excellent writing and editing skills to join our growing team. Recommended coursework: Journalism, newspaper, creative writing, professional writing, editing, and publishing.
$27 - $31 an hourInternExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Minimum of 8-10 years of relevant experience in biotech/pharmaceutical industry with at least 5 years of direct medical writing experience. We are seeking a highly motivated, well-organized, and skilled Director or Sr Director of Medical Writing to lead cross-functional teams in content preparation for submission to regulatory authorities; partners closely with key stakeholders, applies critical thinking, scientific writing, data interpretation, and knowledge of regulatory content life cycle.
$218,978 - $274,868 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Doctorate (Ph. D., MD, PharmD) and 12 years of publication planning, writing, medical affairs, medical communications, clinical or medical information experience or Master’s degree and 14 years of publication planning, writing, medical affairs, medical communications, clinical or medical information experience.
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Have basic English speaking, reading, and writing abilities (Bilingual or multilingual individuals are encouraged to apply) Must have a minimum of 6 months of paid professional caregiving experience (non-family) OR be a CNA, HHA, LVN/LPN, or RN.
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Greenhouse Inventory and Accuracy, regularly writing off damaged product in partnership with the Receiver. Responsible for all Greenhouse Sales and Operating cash register/computer following cash handling procedures as established by Tractor Supply Company.
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Demonstrates a thorough knowledge of Good Clinical Practice GCP, Good Pharmacovigilance Practices GVP, Good Laboratory Practice GLP, Good Documentation Practice GDP and ICH E6 R2 compliance requirements.
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Proven experience as a copywriter, with a strong portfolio showcasing email marketing content, marketing materials, and app-related writing. Improved engagement metrics: Through your writing and content strategy we hope to see an increase in content engagement.
$85,000 - $100,000 a yearFull-timeExpandApply NowActive JobUpdated 29 days ago
writing job Company: Crowdstaffing in San Bruno, CA
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