Proclinical is seeking a dedicated Principal Statistical Programmer to become part of a global Biostatistics and Programming team. This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Responsibilities: - Implement effective more »
Liverpool, Merseyside, North West, United Kingdom Hybrid / WFH Options
ecruit
field. Make a significant impact on developing new treatments. Hybrid working (Liverpool HQ/remote). The Person Bachelor's degree in Life Sciences, Biostatistics, Computer Science or similar. Minimum 3 years' experience in clinical data management, ideally in imaging. Experience with imaging data and software (PACS, DICOM). Knowledge more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
and non-trial tasks are aligned with the project specifications Responsibitly for continuous development of own skills and to contribute to the development of Biostatistics Providing programming input to the setup of the trial, including but not limited to the CRF, Trial Validation Plan and Data Flow Plan Ensuring that more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
in a fast-paced environment A 2:1 degree or better in a numerate or science subject, with a relevant PhD degree (e.g. Epidemiology, Biostatistics, Health Data Science) being desirable Excellent grounding in real world evidence with a desire to apply quantitative skills and rigorous science to solving real-world more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
Surrey, England, United Kingdom Hybrid / WFH Options
Planet Pharma
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their more »
approval, pricing, reimbursement, and patient access. • This position is an individual contributor role. • This position is a remote position. • This position is part of Biostatistics, Medical Affairs (MA) statistics, regional Statistics, Methodology & Simulations or Exploratory statistics. Qualifications: • 5+ years' experience within Statistics/Data Science at a pharmaceutical company. • M.S … in Biostatistics, Statistics or related scientific field with proven experience in applying statistical methods in biomedical research, Pharma, CRO, Academia or Healthcare industry. • Good skills in SAS and R required. more »
Director, Clinical Research Physician (CNS) Our client is a Biotech company with a focus on neuroscience drug development with early-stage and late-stage clinical studies, now have approval for a Director, Clinical Research Physician role working within the Clinical more »
My client, an international CRO working with Pharma and Biotech companies, are hiring a Senior Statistician to join their growing team. The role Lead and manage customer projects ensuring high-quality deliverables Analyse clinical trial data and real-world data more »
Metric Search is actively representing a Global Contract Research Organisation with the hiring of a Director Biometrics to lead their Biostatistics and Statistical Programming Function across the UK and potentially EMEA. Our client is a CRO that provide full-service support to biotech, pharmaceutical and medical device companies. As the … Director Biometrics, you will lead both the Biostatistics and Statistical Programming teams with oversight, as well as offering key technical input. We are looking for the ideal candidate to have at least 10+ years of industry experience to be considered for these opportunities. This is a perfect position for an … path opening doors to even more senior roles and responsibilities in the not-too-distant future as they continue to grow. Your responsibilities: Lead Biostatistics and Programming Function Lead Statistical support and potential oversight on entire projects, serving as main point of contact with sponsor(s) Be responsible for several more »
