Job Details
Associate Director Biostatistics
4401
Posted: 24/11/2023
- 195000
- Nutley, New Jersey, United States
- Permanent
We have partnered with a global, award-winning pharmaceutical company who are searching for a driven, highly analytical Associate Director Biostatistics to help support their Biostatistics department with end-to-end clinical study design, analysis, and publication. Working across a range of complex, ground-breaking projects, this position offers you the opportunity to become an integral part of a company striving to improve the practice of medicine worldwide.
What is it like to work here?
What will you be doing?
What do you bring to the table?
What will you get in return?
What is it like to work here?
- You will have the chance to work on several novel, innovative projects within neurology and oncology at one of the world’s leading pharmaceutical companies.
- Experience for yourself what it’s like to work in a company that prides itself on its ethos for excellence.
- Enjoy being part of a dynamic work environment where your voice is truly valued, and high performance is rewarded.
What will you be doing?
- Offer your statistical support to optimise efficiency in the end-to-end design and implementation of clinical trial programs and research projects.
- Use your expertise to lead multiple global trials and execute diverse statistical tasks.
- You are expected to drive excellence from both project lead and, concurrently, team member perspectives – maintaining the highest quality standards whilst achieving timely deliverables.
- Liaise with the relevant regulatory bodies and health authorities and offer statistical support in preparation of all regulatory documents.
- Data analysis, interpretation, reporting, presentation, and publication support.
- Statistical support for analysis datasets, tables, figures and listings.
- Protocol review, CRF design, SAP writing, TLG shells, CSR writing and data management plan reviews.
- Continual cross-collaboration with other study-related personnel including clinicians and CRO statisticians.
What do you bring to the table?
- Master’s or PhD in biostatistics, statistics, mathematical analysis, or related degree.
- Demonstrable Pharmaceutical industry experience.
- Experience with FDA submissions.
- Excellent communication skills.
- Strong working knowledge of SAS or R.
What will you get in return?
- Clear career progression and development pathways.
- Competitive salary (dependent on experience).
- Benefits – 20% bonus, 15k LTI healthcare, 401K.
Robyn O'Toole
Associate Recruitment Consultant