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Senior Biostatistician oncology remote eu/uk

3 months ago

London, United Kingdom ClinChoice Full time

**Title: Senior Biostatistician Consultant**
**Employment type: 12 Month Contract - Extendable**
**Remote in EU/UK/US**

**About ClinChoice**

ClinChoice is a global CRO dedicated to offering high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Some of these services include clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance. ClinChoice has established major delivery centers across US, Canada, China, Europe, India, Japan, and the Philippines. It has over 3,000 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America, and Europe.

Assignments for **Senior Biostatistician Consultant **isto provide Biostatistical support and work on key client deliverables involving designing and analyzing clinical trials.

**Key responsibilities include, but are not limited to**:

- 3+ years’ experience preferred leading late phase studies.
- Modeling experience such as Mixed Models, Cox Models, Kaplan, Mier Estimates, Poison Modeling would be a plus.
- Protocol development including study design, sample size estimation, randomization, and statistical analysis plan for assigned studies.
- Statistical oversight to studies and assure adequate quality and consistency with project requirements.
- Responsible for accuracy and completeness of database quality checks and assuring that data for statistical analyses are complete, accurate and consistent.
- Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
- Responsible for validity of analysis and alternative analysis strategies when unforeseen circumstances arise.
- Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and corrects flaws in scientific reasoning and statistical interpretation.
- Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.
- Responsible for statistical methods section for the reports. Identifies and corrects flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.
- Effectively coordinate assignments and review deliverables so that projects are delivered on time with high quality.
- Other duties and responsibilities as required and depending on specifics of client projects

**Requirements**:

- MS or PhD in Statistics, Biostatistics or related field. Ph.D. with 4+ years of related experience.
- High degree of technical competence and communication skill, both oral and written.
- Competent in experimental design, descriptive and inferential statistics.
- Pharmaceutical, CRO, or related industry experience with clinical trials.

**Clinchoice is an Equal opportunity Employer/committed to diversity**

Pay: £30.00-£35.00 per year

Schedule:

- 8 hour shift
- Monday to Friday

**Education**:

- Master's (required)

**Experience**:

- SAS: 5 years (required)
- Clinical trials: 3 years (required)
- oncology: 5 years (required)

Work Location: In person