Oncology Scientific Lead, Med Com (Associate Scientific Dir) IREOncology Scientific Lead, Med Com (Associate Scientific Dir)Raleigh, North CarolinaRemoteDemonstrable history of relevant high-level writing support and review (e.g, while at a medical communications agency), including proficiency with ICMJE and GPP guidelines; reviewing and interpreting scientific and technical journal content; knowledge of diverse prescribed styles and formats. This role encompasses high-level writing, peer-review of project deliverables, strategic support and client engagement as determined by the respective aligned account leaders.
NewPrincipal Medical Writer ProPharma Group Holdings LLCPrincipal Medical WriterRaleigh, NCWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Senior Medical Writer (Remote) MMSSenior Medical Writer (Remote)Raleigh, NCRemoteFull timeWrite and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals. Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
NewSenior Medical Writer/Principal Medical Writer - Regulatory Writing Thermo Fisher ScientificSenior Medical Writer/Principal Medical Writer - Regulatory WritingMorrisville, North CarolinaThe Senior Medical Writer provides high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients and demonstrates subject matter and therapeutic area expertise. Serve as primary author who writes and provides input on routine documents such as clinical study reports and study protocols, and summarizes data from clinical studies.
Science Curriculum Designer, Print & Instruction IXL Learning IncScience Curriculum Designer, Print & InstructionRaleigh, NCAs a Science Curriculum Designer for the Print & Instruction team, you'll help guide the development of worksheets and activities for elementary and middle school science (grades K-8) for Education.com, working with contract writers and worksheet creators to produce engaging, high-quality materials. IXL Learning, developer of personalized learning products used by millions of people globally, is seeking an experienced, passionate educator to join our team as a Science Curriculum Designer and help shape our exceptional K-8 science content.
Senior Bioinformatics Data Engineer (Consultant) ProPharma Group Holdings LLCSenior Bioinformatics Data Engineer (Consultant)Raleigh, NCWith deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies.
Vice President, Clinical Development Grifols SAVice President, Clinical DevelopmentNCWith responsibility across a diverse therapeutic portfolio and modalities - including plasma-derived products and recombinant proteins - this role offers a rare opportunity to build future-ready development capabilities, influence portfolio strategy, and lead teams that translate deep biological insight into medicines that meaningfully improve patients' lives. Author and deliver high-quality clinical regulatory documents: Lead the planning, writing, and review of key documents including clinical study reports (CSRs), protocols, investigator brochures, briefing packages, and regulatory submissions, ensuring clarity, scientific rigor, and compliance with ICH/GCP and regulatory guidelines.
Senior Biostatistician - Remote (US) MMSSenior Biostatistician - Remote (US)Raleigh, NCRemoteFull timeLeads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.
Open Rank University of North Carolina at Chapel HillOpen RankChapel Hill, NCDepartment Physics and Astronomy - 319000 Posting Open Date 11/07/2023 Application Deadline Open Until Filled Yes Position Type Permanent Faculty Working Title Open Rank Appointment Type Tenured/Tenure Track Vacancy ID FAC0004835 Full-time/Part-time Full-Time Permanent Hours per week 40 FTE 1 Position Location North Carolina, US Hiring Range Proposed Start Date 07/01/2024. University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events.