inVentiv Health Clinical (formerly known as Pharmanet i3) is currently recruiting for a number of positions in Statistics and Statistical Programming functions.
The positions are working within our inVentiv Health Clinical, Strategic Resourcing Division and are fully dedicated to a single pharmaceutical client/sponsor.
The positions are full time and can be offered either as a freelance contract for 12 months (renewable), or through permanent contracts of employment. Excellent rates of pay or a competitive salary (plus benefits) are on offer for candidates with the right experience.
Senior Statistician
Home Based, Western Europe
Working as Senior Statistician, your responsibilities will primarily be focused on design and modelling.
Requirements:
Proficient knowledge of / experience with SAS, R, S plus or any other business or research analytic software
Proficient in up-to-date statistical knowledge/applications and advanced expertise in analytic aspects including simulations, modeling and Bayesian techniques
Solid experience in leading statistical analytic support for multiple trials
Proven knowledge in drug development
Deep knowledge of data architecture
Senior SAS Programmer
Home Based, Western Europe
Requirements:
Advanced knowledge of / experience with SAS and other relevant programming software.
Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills
Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent)
Working knowledge of database design/structures and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent)
Good understanding of global clinical trial / project practices, procedures, methodologies.
Good understanding of regulatory requirements relevant to statistical programming (e.g. GCP, ICH).
Knowledge of office tools.
Senior Statistician
Office based, Surrey
Working as Senior Statistician, your responsibilities will primarily be as follows:
Provide scientific statistical input to development plans and to project planning.
Provide representation on project teams Make study design recommendations and prepare sample size calculations for Outline Protocols.
Prepare statistical section for Clinical Study Protocols.
Generate the randomization schedules for clinical trials in accordance with the protocols and maintaining security of schedules before and during the studies.
Provide input to the design of Case Report Forms and review Edit Check Specifications.
Preparation of Statistical Analysis Plans.
Interact with statistical programmers regarding programming requirements for analysis and reporting.
Perform statistical analysis and produce derived datasets for statistical output.
Validation/QC of other statisticians’ analysis.
Prepare the statistical section of top line and Final Clinical Study Reports.
Review Clinical Protocols and Final Study Reports.
Senior SAS Programmer
Office based, Surrey
Working as Senior SAS Programmer, your responsibilities will primarily be as follows:
Provide statistical programming support for assigned project
Review protocols, CRF's, statistical analysis plans, and data submission plans
Develop general SAS application code.
Prepare the data package for a regulatory submissions
Validate SAS programs and analysis results
Import and export data files.
Assists in Quality Control activities
Generate and maintain documentation.
Attends project meetings and departmental meetings
Senior SAS Programmer
Office Based, North West England (some flexibility to partly work from home)
Working as Senior SAS Programmer, your responsibilities will primarily be as follows:
Programming in SAS for analyzing data and producing safety and efficacy tables, listings and figures in specified formats for phase I to phase IV clinical trials
Creation and review of programming specifications
Programming in SAS for creation of derived data sets as per the specification document
Performing quality checks for reports generated by other team members and validation of new/ modified SAS programs and macros
Review of clinical study protocol and SAP before starting the actual work on the study (as assigned)
Support the team with training activities, i.e. train other team members on SAP, clinical study protocol, Company’s and/or Client’s SOPs and Working Standards/ Instructions, Regulatory Guidelines, CDISC and ADaM modules, etc.
Responsible for day-to-day work, process flows and constantly endeavoring to be able to set an example
Assist the supervisor by providing the status on: deliverables, study updates such as timelines and any delay from client in providing the raw data/ SAP/ Protocol etc and also discuss the challenges in meeting the timelines or quality of deliverables, if any
To be eligible for consideration you will have proven experience in the CRO/Pharmaceutical industry, working within the field of clinical trials. You will be educated to a minimum of BSc level for a Senior SAS Programmer position, or MSc/PhD for the Senior Statistician role and be able to demonstrate technical competency within the statistical field.
Please apply by CV to [log in to unmask] or telephone +44 (0) 1895 451 806 for a discussion.
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