Cmed is a Contract Research Organisation providing Full Service Solutions for immuno-oncology and cell & gene therapy studies as well as Data Science and Analytics services. We occupy a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials but also as a developer of our own technologies for managing clinical data.
This is a very exciting time to join Cmed as we start to leverage our already considerable expertise in the delivery of clinical trials with encapsia. This unique combination of operational expertise and the latest technology helps reduce the costs and increase the speed of developing new medicines, essential to both improving and saving the lives of patients.
We are currently looking for an enthusiastic and talented Senior Biostatistician to be home/office based in UK/EU.
Your core responsibilities:
To provide expert statistical input to Phase I-IV global clinical trials including the design of clinical trials and the production of analysis and reporting deliverables.
Specification, production and QC of analysis and reporting deliverables including statistical analysis plans and integrated summaries of efficacy/safety.
Statistical programming and QC of analysis datasets containing statistical elements, tables and figures for global phase I-IV trials.
Responsible for the quality and timeliness of statistical deliverables.
As Lead Biostatistician, to be primarily responsible for all statistical activities on allocated studies including planning and coordination of activities for assigned statistical team members.
This position is perfect for you if you have:
A Masters (M.Sc.) (or equivalent) in Medical Statistics or a degree (or equivalent) in Statistics/Mathematics in conjunction with demonstrable experience as an applied Statistician at a pharmaceutical company, CRO or academic institution.
Strong experience of project managing statistical activities as a Lead Biostatistician (including timelines, forecasting, budgets and client interactions), ideally at a CRO.
Expert knowledge of clinical trial practices, procedures and methodologies, and the statistical principals underlying them.
Strong experience of performing reviews of integrated summaries of efficacy/safety data as Lead Biostatistician. Ideally experience in performing independent/senior review.
Strong oral and written communication skills.
Good SAS programming abilities.
The ability to work independently as well as with colleagues.
Ideally experience in providing statistical input into study protocols and sample size calculations.
Ideally experience in Oncology trials.
Ideally experience in Real World/Observational studies.
Ideally experience and knowledge in Bayesian adaptive designs.
Ideally experience in providing deliverables for Data Monitoring Committees (or equivalent) and attendance at meetings.
What we offer:
Opportunity to be part of an innovative organisation and work with exciting technologies.
Mentoring and training to develop your skills in the clinical trials industry.
The chance to be part of an effective, friendly and supportive team.
Competitive employment package.
For more information on Cmed recruitment and consideration for other opportunities, please review the recruitment statement on our careers page (https://www.cmedresearch.com/careers/).
Please be aware that we do not accept resumes from outside agencies or recruiters unless specifically requested by a Cmed HR or Recruitment Manager. Unsolicited agency or recruiter resumes will not be eligible for referral fees and will be considered candidates Cmed may directly contact for employment application.