Description
We are seeking an Associate Principal to lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions. As an Associate Principal, you will be a methodologic expert with substantial experience in providing consulting services to Pharmaceutical clients.
Responsibilities:
- Lead implementation of evidence synthesis projects from pre-award to final delivery
- Lead project teams to ensure high-quality deliverables according to timelines
- Synthesize data qualitatively and quantitatively, and guide junior staff
- Manage projects, oversee operational, financial, and administrative requirements
- Independently qualify leads, develop proposals, attend bid defenses, and manage contracting
- Support senior staff on business initiatives as required
- Work effectively across time zones as part of a global team
Qualifications, Experience, Technical and Personal Skills:
- Master's in epidemiology or biostatistics (or other health sciences)
- 7+ years of experience implementing evidence synthesis research in a pharma consulting environment
- PhD in epidemiology or biostatistics (or other health sciences) preferred
- 5+ years of experience as client point of contact on projects
- Significant experience with Bayesian NMAs, ITCs, and meta-analysis
- Solid understanding of SLR concepts, guidelines, and required rigor
- Strong ability to quality check own and others' work
- Exceptional attention to detail
- Fluency in English (spoken and written)
- Commitment to working collaboratively and effectively with others
- Pragmatic and logical problem-solving approach
Benefits:
- Competitive salary ($125,800 - $350,300 per year)
- Range of health and welfare benefits