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 »
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 »
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 »
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 »
teams Serve as a line manager for junior staff members Qualifications, experience, technical and personal skills Essential qualifications Master s degree in (medical) statistics, biostatistics, mathematics, epidemiology, public health, health economics or a related discipline PhD in a subject related to health services research or statistics is desirable Essential skills more »
Mentor junior colleagues Contribute to internal training initiatives, process improvement, and business development Key Skills and Requirements: Be passionate about statistics University degree in Biostatistics or a similar related field Knowledge of HTA-related methods, including ITC, NMA, and complex statistical modelling techniques Awareness of regulatory standards, ICH/GCP more »
and meta-analyses to support the development of protocols and evidence-gap analyses. PhD in economics/health economics, pharmaceutical outcomes and policy, statistics, biostatistics, decision sciences, health services research, Strong communication skills (written and oral) Willingness to partner with cross-functional stakeholders at global and regional levels Robust experience 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 »
analyses to support the development of protocols and evidence-gap analyses. Required Qualifications: PhD in economics/health economics, pharmaceutical outcomes and policy, statistics, biostatistics, decision sciences, health services research, biology, or a related field with a minimum of 3 years of experience in the pharmaceutical industry, contract research, or 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 »
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 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 »
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 »
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 »
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 »
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 »
area of specialism considered, Oncology also advantageous. How you will be a success The Principal Biostatistician will be accountable for the leadership of the Biostatistics and Programming activities of a program of studies of moderate complexity and/or of high value with high impact for the organization. Also responsible … regulatory questions on the design of the program, and any labelling claims following submission Participates in presentations at client and investigator meetings. Preparation of biostatistics input to company research proposals and participates in proposal defense meetings and makes presentations at marketing meetings with prospective client. Key Qualifications and Skills M.S. … or Ph.D. degree in statistics, biostatistics, or related field. Experience in statistics, biostatistics or related field Accountable for leading Biostatistics and Programming activities for a program of studies of high complexity and/or of high value with high impact. Bio statistical input into the design of the program, Protocol more »
