Offer summary

Qualifications:

Advanced degree in biostatistics, computer sciences, or a related field (Doctoral degree preferred)., 8+ years of experience as a Lead Biostatistician in biotech, CRO, or pharmaceutical settings., Proficiency in SAS and statistical procedures for data analysis., Strong communication skills and knowledge of the observational study process..

Key responsabilities:

Lead complex RWE studies and coordinate activities across multiple locations.

Develop and review Statistical Analysis Plans (SAPs) and conduct statistical reviews of study outputs.

Present findings at team meetings and external conferences, sharing knowledge with peers.

Act as a Subject Matter Expert, developing procedural documents and participating in bid defense meetings.

Job description

Sr Biostatistics Manager RWE

As an experienced Sr Biostatistics Manager RWE in our Consulting business supporting our Real-World Evidence (RWE) service, you are central to the successful delivery of complex RWE studies for renowned, innovative and global top pharmaceutical and biotech companies. You will have the opportunity to lead RWE studies and support post-market regulatory submissions and publications.

In this role you will develop and review Statistical Analysis Plans (SAPs) for data presentation, analyses, and provide SAS programming oversight.

What else can you expect from us?

Rewarding and meaningful work in an established, diverse, highly profitable and respected global company
Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances etc.
A genuine work life balance
Flexibility in working hours
A thorough onboarding with support from your personal mentor
A permanent employment contract with Fortrea
Excellent training and career development opportunities, as well as support with advancing your individual education

Your responsibilities:

Lead complex studies or complex, multi-protocol programs, potentially coordinating activities across multiple locations, providing statistical oversight and attending relevant project meetings
Lead the development of complex SAPs perform senior review of SAPs developed by other statisticians
Conduct overall statistical review of Tables Figures and Listings for complex studies prior to client delivery
Develop the statistical sections of the protocol for complex studies under the supervision of a statistical consultant
Present and share knowledge at monthly team meetings and at external scientific meetings and conferences
Attend bid defense meetings
Act as Subject Matter Expert and develop or review procedural documents, or work on new initiatives

Your profile:

Advance degree in a relevant field such as biostatistics, computer sciences, etc. (Doctoral degree preferred)
8 or more years of solid experience of working as a Lead Biostatistician in either a biotech, CRO or pharmaceutical company
Ability to program in one or more statistical software packages (SAS®) used to conduct statistical analyses; SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis
Proven professional experience with SDTMs, ADaM datasets and TFLs
Proven ability to effectively communicate statistical concepts
A good knowledge of the overall observational study process
Competence in the preparation of SAPs, analysis, and reporting
Strong organizational skills, an autonomous and collaborative work style, a curious mind and a keen attention to detail

Learn more about our EEO & Accommodations request here.

Required profile