Associate director biostatistician

Job summary:

A great opportunity for an experienced biostatistician to be a prominent leader in the clinical trial process. You'll be able to play an integral part in consulting with different biostatistician and offering leadership and guidance and will be working on some of the biggest projects in the field. You'll be able to gain the experience of participating in the client management and sales, proposals, and budgeting side of the clinical trial process. This is a great chance to progress and take on a challenging new opportunity.

Requirements:

• Able to work in the UK and Europe
• Ideally you will have previous experience working in a CRO and/or pharmaceutical organisation in the past
• Ideally will be able to engage with stakeholders and sponsors, consulting on the proposal phases of clinical trials
• Must have and sufficient understanding and experience working with SAS. Knowledge of other programs like R, python, SPSS, STATA are preferred but not required.
• Able to lead multiple projects simultaneously with varied therapeutic areas
• Experience with dealing with clients closely and understanding trial expectations in preferred
• Entitled to work in the UK and Europe

Other benefits:

• You'll have the opportunity to progress quickly within the organisation and be in a leadership position from the start.
• Competitive salary
• Remote working
• You'll be able to build great client relationships
• You'll have the opportunity to work for a company that has recently been nominated for thr best company to work for 2021

Get in contact with James Bruce to have a confidential conversation, 0207 551 0805, jbruce@i-pharmconsulting.com

ABOUT I-PHARM CONSULTING:

I-Pharm Consulting is a specialist Recruitment Company servicing the pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

Keywords:

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