inVentiv Health are hiring!
Here at inVentiv Health we have opportunities for both Statisticians and Statistical Programmers and can consider flexible options, depending on the candidate and experience level.
Please see below details and get in touch with Gemma Green to discuss further if you are interested.
Senior Statistician
Full-time. Freelance or Permanent. Home or office based.
Responsibilities:
Provide scientific statistical input to development plans and to project planning.
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 Topline and Final Clinical Study Reports.
Present and discuss results with internal/external bodies as required.
Review Clinical Protocols and Final Study Reports.
Approve Case Report Forms.
Eligibility/Qualifications/Requirements
MS or PhD in Statistics (or related) with solid pharmaceutical industry experience working on clinical trials
Submissions experience to the FDA or regulatory body
Excellent communication and interpersonal skills
Ability to lead projects and work within a matrix environment
Senior SAS/Statistical Programmer
Full-time. Freelance or Permanent. Home or office based.
Responsibilities:
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
Eligibility/Qualifications/Requirements
SAS Programming experience in the CRO/Pharmaceutical industry and a degree in a related field.
You should have solid experience of coding analysis datasets and tables, listings, graphs programs from scratch and good documentation skills are desired.
Both positions are great opportunities to join a global pharmaceutical business. You will be part of the consumer health team and will be responsible for multiple international studies.
If you have the required experience for either position and are eligible to work in the UK then please reply with your updated CV to [log in to unmask]
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