Principal Biostatistician
- Employer
- Albion Rye Associates
- Location
- Greater Boston Area (Remote work considered), East Coast
- Salary
- $140,000 - $175,000 depending on experience + benefits package & bonus
- Start date
- 1 Apr 2021
- Closing date
- 1 May 2021
View more
- Discipline
- Data Management / Statistics, Data Analyst, Biostatistics, SAS Programming, Statistical Programming, Statistics
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Principal Biostatistician
$150,000 – $170,000 depending on experience + comprehensive benefits package
Greater Boston Area, MA – East Coast (Remote work considered)
Albion Rye Associates are working in partnership with our client, a well-respected leading Biotech, in the recruitment of a Principal Biostatistician acts as the study statistician for multiple clinical studies and/or as the statistical lead for a clinical development program.
You will provide leadership and guidance on designing studies, selecting appropriate and innovative statistical methods, analyses, interpretation, and reporting of study results. Participate in regulatory interactions and submissions to the regulatory agencies; Contribute to the biometrics work across the organisation to identify, develop and implement standards, applications, processes, and training.
Principal responsibilities will include to:
- Work with the internal and external stakeholders on design and execution of clinical trials in the organisation’s portfolio.
- Partner with the Statistical Programming team in the generation of statistical analyses for internal and external presentations, and validation of statistical analyses results generated by CROs and vendors.
- Collaborate in the reviewing of CDISC electronic data packages for completeness, regulatory agency standards compliance and submission.
- Oversee the execution of the statistical components by CROs and vendors. Manage timelines and quality deliveries of generated statistical analyses results.
- Keep up with regulatory requirements for statistical methods of analyses and scientific developments in statistical methods for clinical trials.
- Consult with the internal audit team in evaluating regulatory compliance with respect to statistical SOPs.
Your Background:
- PhD in Statistics, Biostatistics, or Mathematics with a minimum of 3 years (minimum 5 years for MS degree) PhD of experience in clinical trial development.
- Proven ability for project management of projects in clinical development, with experience managing delivery of statistical projects by CRO and vendors.
- Knowledge of global regulatory guidance on statistical methods for analyses of clinical data, and global submission requirements.
- Ability to apply complex statistical methods, conduct and interpret the results.
This role will be based in the East Coast with a preference to the Greater Boston Area. Although other locations will be considered too.
Please get in touch with Erick Semerene, Head of Biometrics Recruitment:
Email: erick.semerene@albionryeassociates.com
Phone: +1 (857) 930-7567
ALL CONVERSATIONS ARE HELD IN THE STRICTEST CONFIDENCE
Company
At Albion Rye Associates, we create a bespoke recruitment process that is thorough, professional, personable – and most importantly, tailored to exactly to what you need.
We have a clear focus on collaboration and communication. We are solutions-led and know from vast experience that for successful outcomes to be reached, we don’t just work for our clients and candidates – we work with them.
Our valued clients and candidates have the highest of standards and expectations. We are exactly the same. If we weren’t, they wouldn’t want to work alongside us. We ensure that every client and candidate receives the made-to-measure, personalised recruitment service that they want, need, and deserve through building long-term working relationships.
- Website
- https://www.albionryeassociates.com/
- Location
-
CoTribe Offices – Raven House
29 Linkfield Lane
Redhill
Surrey
RH1 1SS
United Kingdom
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