focused driven individuals for SAS Programmer role to be office-based in London UK. This is a vital role in our Clinical Database Programming & Biostatistics department whose success hinges upon your attention to detail and programming background. At Medpace, our SAS Programmers go through an extensive onboarding and training process more »
enable consistent and efficient project deliverables across portfolios; developtools for efficient production and verification of derived datasets, e.g. SDTM and ADaM, and TLFs Collaboratewith Biostatistics to develop, implement and maintain appropriate statistical applications such as data review and reporting tools and provideprogramming support to the regulatory submissions including data submission more »
This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board. Overview Head of Biopharma Biostatistics - Remote UK Remote The Emmes Company, LLC ("Emmes") is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public … from entry level through top executive - to contribute to our clients' success by sharing ideas openly and honestly. Primary Purpose The Head of Biopharma Biostatistics serves as a leader within the global biostatistics department responsible for strategic and operational oversight of the biostatistics and statistical programming activities for Emmes' biopharma … key therapeutic areas such as vaccine and infectious diseases, ophthalmology, CNS, rare disease and cell and gene therapy among others. The Head of Biopharma Biostatistics serves as a member of Emmes' biopharma leadership team ensuring high-quality, on time, and on budget statistical deliverables and supporting business development activities for more »
and efficient project deliverables across portfolios; develops tools for efficient production and verification of derived datasets, e.g. SDTM and ADaM, and TLFs. Collaborates with Biostatistics to develop, implement and maintain appropriate statistical applications such as data review and reporting tools. Provides programming support to the regulatory submissions including data submission more »
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 »
appropriately coordinating assignments and reviewing work so that projects are delivered on time with high quality. Education and Experience: MS or PhD in Statistics, Biostatistics or related field. PhD with 3-5 years of experience or MS with 6-8 years of experience. Experience with V&I therapeutics. Strong oral more »
and plans integrating, analysing, and interpreting datasets to provide evidence to progress the portfolio across both therapeutic areas Experience: Ph.D. in Bioinformatics, Computational Biology, Biostatistics, or related field with 3+ years of post-degree experience Strong programming/scripting skills in R and/or Python, as well as experience more »
Proclinical is seeking a dedicated and innovative Principal Statistician to join a dynamic team. This role will focus on leading the Biostatistics activities for a program of studies of moderate complexity. The successful candidate will be responsible for ensuring the delivery of individual studies and the overall program on time … and to the required quality. This role is an excellent opportunity to contribute to our mission of advancing and improving patients' lives. Responsibilities: Leading Biostatistics and Programming activities for a program of studies. Providing biostatistical input into the design of the program, including study design, sample size calculations, and patient … to regulatory questions on the design of the program, and any labelling claims following submission. Participating in presentations at client and investigator meetings. Preparing biostatistics input to research proposals, participating in proposal meetings and making presentations at marketing meetings with prospective clients. Providing ongoing coaching and mentorship to team members. 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 »
and efficient project deliverables across portfolios; develop tools for efficient production and verification of derived datasets, e.g. SDTM and ADaM, and TLFs Collaborate with Biostatistics to develop, implement and maintain appropriate statistical applications such as data review and reporting tools and provide programming support to the regulatory submissions including data 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 »
and efficient project deliverables across portfolios; develops tools for efficient production and verification of derived datasets, e.g. SDTM and ADaM, and TLFs. Collaborates with Biostatistics to develop, implement and maintain appropriate statistical applications such as data review and reporting tools. Provides programming support to the regulatory submissions including data submission 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 »
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 »
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 »
ophthalmic setting Knowledge and Training Essential Standard keyboard skills Desirable Previous experience using related ophthalmic technology eg Humphrey Visual fields, OCT, Corneal Topography and Biometry Willingness to attend training courses (internal and external) and complete all mandatory training as required by the role Communication & Relationship Skills Essential Good communication skills more »
