Overview
About the Manager Position:Analysis Group is seeking an experienced professional to support the continued growth of our clinical trial and biostatistics capabilities. This role is suited for candidates with a strong foundation in clinical trial data, statistical programming, and regulatory processes who are interested in applying their expertise in a consulting environment.
Managers play a key role in leading analytical workstreams, guiding project teams, and contributing to strategic decision-making across a diverse portfolio of client engagements. Responsibilities may include:
- Apply biostatistical methods to support clinical development, regulatory submissions (e.g., FDA, EMA), and evidence generation strategies
- Contribute to strategic advising on clinical trial design, analysis strategy, and interpretation of results Oversee implementation of statistical analysis plans (SAPs) and ensure high-quality, reproducible analytical outputs
- Manage and mentor teams of analysts and associates, providing guidance on technical execution and professional development
- Direct data integration, cleaning, and transformation efforts across clinical trial and real-world data sources
- Develop tools, programming standards, and best practices to enhance efficiency and scalability of analyses
- Communicate findings to technical and non-technical audiences, including translating complex analyses into clear, actionable insights
- Contribute to business development efforts and support ongoing client relationships
- Participate in dissemination of research through publications, presentations, and regulatory documentation
Analysis Group fosters a work environment that is centered on delivering high-quality work through teamwork and collaboration, best-in-class learning programs, and a culture of transparency, trust, and respect. We are looking for candidates who demonstrate both technical expertise and strong interpersonal skills, and who are passionate about applying data and analytics to real-world challenges in the life sciences industry. Specifically, we seek candidates with:
- Advanced degree (PhD preferred, Master’s considered) in Biostatistics, Statistics, Epidemiology, or a related quantitative field
- Approximately 3–5+ years of relevant experience in clinical trials, pharmaceutical, biotech, or CRO environments
- Experience in early- to late-phase clinical trial design and regulatory evidence strategy
- Experience supporting or contributing to clinical phase regulatory submissions for the US FDA and other regulatory authorities. Direct participation in regulatory interactions is a plus.
- Excellent judgement, problem-solving, and communication skills, with the ability to translate complex technical concepts into clear, structured insights for clients
- While prior consulting experience is not required, candidates should demonstrate strong potential for client-facing work and structured problem solving
- Prior experience collaborating across cross-functional stakeholders (e.g., clinical, regulatory, HEOR)
- Experience managing analyses, including SDTM, ADaM, and TLF development
- Demonstrated ability to manage multiple workstreams and meet deadlines
- Interest in mentoring and developing junior team members
- Collaborative mindset and ability to work across interdisciplinary teams
- While not required, a plus would be experience with post-marketing evidence generation, including label expansion strategies, PASS/PAES, Phase IV studies, and the use of real-world evidence to support regulatory decision-making
Candidates must be legally authorized to work in the United States at the time of hire. Analysis Group may consider candidates who require visa sponsorship, consistent with business needs.
Analysis Group offers competitive compensation and a comprehensive benefits package. The estimated salary range for this position is $210,000–$255,000. Compensation offered will be based on a number of factors including work experience, education, and skill level. This role is eligible for a discretionary annual bonus that is determined in large part by individual performance. To learn more about our benefit offerings, click here.
