Contract Senior Statistical Consultant
Based in Middlesex or Cambridge
Our client is a leading Fortune 500, Biotechnology Company. With headquarters in the USA, my client employs over 500 staff in their UK offices, located in Cambridge and Middlesex on both a permanent and contract basis.
A market leader, my client strives to develop products that change people's lives and in the last 30 years have transformed the management of anaemia, inflammation, and cancer. They have a thriving pipeline and are currently very active in recruiting candidates to join the team on a contract basis.
Both UK sites are easily reachable by mainline BR and have excellent road links with ample free car parking.
Our client knows they offer a great place to work. Our client understands that each candidate is not the same, and no two roles are either. That's why they permit up to two days working from home per week depending on the role. Moreover, it's a place where^you will be more than a contractor- you will be one of the team, and that even means an early Friday finish!
This role will suit a capable medical statistician who has industry or CRO based experience in acting as a function lead and project statistician on clinical trials. You will be assigned studies across Phases II-IV and contribute from design and plan stage to analysis and reporting. The work to be assigned includes ongoing projects in pediatric indication and CVS/Endocrine medicine.
We are looking for a capable statistician who has experience in design, analysis and reporting clinical trials within a regulatory driven environment. This role demands proficiency from Day 1 so we are unable to consider statisticians who do not have pharmaceutical experience.
In this role you will work within an expert pharmaceutical company team who are focused on both interventional and observational research there may be scope to expand your knowledge and remain beyond the 6 month initial assignment. This organisation treats contractors as a key contributors and there is significant flexibility and trust often enabling candidates living far remote to adopt a 3 day in-house based schedule after successful orientation.
This is a^contract for 6 months initially CSL can offer PAYE or a contract based arrangement on a Day Rate. We may consider candidates who wish to work 4 days as a back up so do apply if you seek this flexibility. The rate is negotiable.
The role can be based at our clients West London or Cambridge offices, which there is a core hours policy.
Prepares analysis plans and writes detailed specifications for analysis files, consistency checks, tables, and figures; communicates with clients regarding statistical analysis issues.
Interprets analyses and writes statistical sections of study reports. Has knowledge of commonly-used concepts, practices, and procedures within a particular field.
Relies on instructions and pre-established guidelines to perform the functions of the job. Works under immediate supervision.
Typically reports to a supervisor or manager.
Skills & Qualifications Required
MS degree in statistics, biostatistics, or related field
Relevant recent^pharmaceutical or related statistical experience
Right to Work by EU nationality of a visa valid for the period of the assignment
Candidate living in the UK will be considered as the priority
Software Competence Required: SAS experience
Employer: Pharmaceutical Company via agency
Employment Type: Agency Contract
Hours: Full time, client may consider 4 days per week for an exceptional contender
Initial Contract Term: 6 Months
Location: M4 West London, Cambridge, UK
Plan Start Date: ASAP.
Pharmaceutical, Clinical study, Manager, SAS,Statistician, Statistical Analysis, ANOVA, WinNonlin, SPSS, Clinical Study Report, CSR, biostatistics, MSc, EU, Cambridge, London
Assigned Consultant: Sue Spice at CSL on 01932 228 928
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within 24hrs, applicants will only receive feedback if they are suited to the role. If you applied for this role previously and were unsuccessful you will not receive a response. We are unable to respond to applicants who are not EU nationals unless they include evidence of right to work in full time employment with their application. Do apply with relevant information on^required location location or salary/day rate if you are a new candidate.