Remote Biostatistician for Clinical Trials & Submissions
Full time
Hire Feed
pHire Feed is hiring a Biostatistician to work remotely on a full-time basis, analyzing clinical trial data and designing statistical methodologies for regulatory submissions. /ppThe role requires SAS/R/Python proficiency, experience with clinical trials and FDA/EMA guidelines, and the ability to communicate complex results to non-statistical stakeholders. This is a remote, global opportunity with cross-functional collaboration. /p #J-18808-Ljbffr
Offerta di lavoro pubblicata 2 giorni fa
Offerte di lavoro simili
- pHire Feed is seeking a Biostatistician to work remotely on full-time basis. You will analyze clinical trial data, design... ...and prepare reports for health authorities,... ...experience with regulatory submissions, and ability to... ...statistical stakeholders in a remote, work-from-anywhere...RemotoTempo pieno
- pHire Feed is seeking a Biostatistician to join a remote, full-time role focused on clinical trial data analysis and regulatory compliance... ...Python, and prepare reports for health authorities. /... ...objectives are met and to support submissions across therapeutic areas. /p...RemotoTempo pieno
65.000 €
...ensuring rigorous analysis of data from clinical studies and related analyses. You will work... ...Medical Writing and other functions for scientific clarity, consistency, and regulatory... ...contributing to major regulatory submissions (NDA, MAA or equivalent) and responding...Consigliato- ...Senior / Principal Biostatistician Statistical Programmer / Technology... ...pharmaceutical company, is looking for a Principal Biostatistician... ...programming activities for clinical trials (Phase I-IV) or large global... ...with a hybrid / remote work model based in Italy...RemotoLavoro ibridoOrario flessibile
- pstrongSenior / Principal Biostatistician Statistical Programmer / Technology... ...company, is looking for a strongPrincipal Biostatistician... ...programming activities for clinical trials (Phase I-IV) or large global... ...with a stronghybrid / remote work model /strong based in...RemotoLavoro ibridoOrario flessibile
- pWarman O'Brien is seeking a Principal Biostatistician (strong seniors considered) to shape... ...will lead statistical strategy across clinical trials and collaborate with cross-functional... ..., and support inspections in a hybrid/remote Italian work model. /p #J-18808-LjbffrRemotoLavoro ibrido
- ...Syneos Health is seeking a Principal I/II Medical Writer (Clinical / Submissions exp) for fully remote work across Europe (Italy, UK, Spain, Poland or Ireland). The role focuses on regulatory submissions, medical writing deliverables, and collaborative partnership with...Remoto
- ...ll Do: Serve as main CTI contact for assigned study sites Conduct site... ...all Investigational Product (IP) and trial-related materials Perform site... ...provide ongoing updates of site status to Clinical Project Manager Conduct remote monitoring and complete related...RemotoLavoro ibrido
78.000 € - 100.000 €
...challenging full-service global clinical research projects, managing... ...every aspect of the study. Remote or Hybrid Your responsibilities... ...or equivalent (e.g. Clinical Trial Manager, Clinical Study Team... ...Information The gross salary range for this role is 78,000-100,000...RemotoTempo pienoLavoro ibrido- ph3bPrincipal Biostatistician (strong Seniors considered) - Global Pharma... ...company, is looking for a bPrincipal Biostatistician... ...about designing meaningful clinical trials and influencing global health... ...flexibility with a bhybrid / remote work model /b based in Italy...RemotoLavoro ibridoOrario flessibile
- pstrongPrincipal Biostatistician (strong Seniors considered) - Global Pharma... ...company, is looking for a strongPrincipal Biostatistician... ...about designing meaningful clinical trials and influencing global health... ...with a stronghybrid / remote work model /strong based in...RemotoLavoro ibridoOrario flessibile
- ...Overview As Medical Director you provide medical oversight for clinical trials and serve as the primary medical monitor for sponsor-led... ...study protocols, ICFs, CRFs, analysis plans, and regulatory submissions Ensure activities align with GCP and operate efficiently...Lavoro da casaTurni
- Job SummaryMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial... ...to expand to a new therapeutic area. We provide remote flexibility only with relevant experience (after...RemotoLavoro da casaOrario flessibile
- ...Are you an experienced Clinical Research Associate looking to join... ...across Italy, ensuring clinical trials are conducted in accordance... ...ethics committee and regulatory submissions where required. Monitor... ...site performance. Maintain Trial Master File (TMF)...Lavoro da casaOrario flessibile
- ...post-approval activities focused on CMC for vaccines or biologics. The role allows office... ...work across Europe. /ppYou will develop submission strategies, assess change controls,... ...management systems. Fluent English required; remote options available. /p #J-18808-LjbffrRemotoLavoro da casa
- ...interested in working directly for a single sponsor while having... ...ppClinChoice is searching for a Clinical Supply Chain to join a... ...operation) /liliWorking model: remote/hybrid acceptable; occasional... ...liliProven experience in clinical trial supply operations (phases (I/II...RemotoTemporaneoLavoro ibrido
28.000 € - 34.000 €
.../ppbr/ppstrongIn-House Clinical Research Associate /strong... ...— in presenza e da remoto — gestendo l'allocazione... ...diretto su studi condotti in remote monitoring/on-site... ...Manager e Clinical Trial Assistants. /li /ulpbr/... ...di CRA / monitoraggio clinico. /liliEsperienza pratica...RemotoLibero professionistaContratto con partita IVALavoro ibrido- ...this role you lead medical, scientific, and strategic direction for clinical trials and act as the internal medical expert for study results. You... ...and with sponsors to support proposal development and trial execution. You will help translate findings into regulatory and...Lavoro ibridoLavoro da casaOrario flessibile
- ...statistical strategy for complex client studies... ...to shape cutting-edge trial designs. Responsabilità... ...guidelines and global submission expectations (FDA, EMA... ...as an independent biostatistician on DSMBs and DMCs Requisiti... ...years' experience in clinical trials design and...
- ...role you steer the global clinical development strategy for key respiratory indications... ...commercial goals, shape trial designs, and drive regulatory... ...flexible working remote working relocation support... ...documents and major regulatory submissions Requisiti fondamentali...RemotoOrario flessibile
- A forward-thinking AI firm is seeking a Statistician with Python skills for a remote freelance role. The position involves generating AI prompts, defining scoring criteria, and correcting model responses based on statistical expertise. Candidates must hold a relevant degree...RemotoPart-timeLibero professionista
- ...Linical Europe is seeking an experienced Clinical Research Associate II to manage investigative sites across Italy, ensuring trials follow protocol, ICH-GCP and regulatory requirements. You will perform site qualification, initiation, monitoring and close-out visits from...RemotoLavoro da casa
- ...Warman O'Brien seeks an experienced Principal Biostatistician Statistical Programmer / Technology Lead to shape drug development and lead programming for global trials in a hybrid Italy-based setting (Milan). The role emphasizes CDISC SDTM/ADaM compliance, regulatory readiness...Lavoro ibrido
34 $/ora
...with Python - Freelance AI Trainer This opportunity is only for candidates currently residing in the specified country. Your location... ...challenging, complex guidelines. Our freelance role is fully remote, so you just need a laptop, internet connection, time available,...RemotoPart-timeLibero professionista118467 $
...This Job is based in Australia Research Fellow (Biostatistician) - The Kirby Institute Employment Type: Full - time (35 hours a week)... ...loading Work rights required: Visa sponsorship is not available for this position. Candidates must hold full rights to work in...Tempo pienoTempo determinatoOrario flessibile- ...UNSW’s Kirby Institute seeks a Research Fellow (Biostatistician) to design, analyze and report on linked health data studies. You will apply... ...career development path and opportunities to contribute to high-impact health research for Australia and globally. #J-18808-Ljbffr
- ...scientific support to clinical research programs, study... ...advice, and leadership for potentially or awarded... ...oversight for clinical trials by serving as Medical Monitor... ..., regulatory approval submissions, serious and non-... ...medical practice (hospital/clinic), academia, clinical...Part-timeTempo pienoDisponibilità immediataLavoro da casaTurni
33.000 € - 49.400 €
...the market. We are looking for a Regulatory Affairs Analyst... ...lifecycle activities, regulatory submissions and client support while... ...a hybrid position, combining remote working with attendance at the... ...a leading global provider of clinical research services, commercial...RemotoPart-timeTempo pienoTempo determinatoLavoro ibrido- ...over €1.5 billion in monthly transactions for more than 150 companies—like Pennylane,... ...regulatory changes in Italy. Regulatory Submissions: Assist in submitting regulatory... ...health and wellness. &##129496; Hybrid remote policy : We offer the possibility of working...RemotoLavoro ibridoLavoro da casa2 giorni/sett.Orario flessibile
23.560 € - 36.813 €
...Description /b /pulliThis position is intended for candidates belonging to Protected... .... /liliItaly, hybrid on site in Turin or Remote /li /ulh3bResponsibilities: /b /h3ulliManage... ...communications and administrative submissions, including areas such as hires, terminations...RemotoSmart workingTempo pienoLavoro ibrido