WHO ARE PRESCIENT?

We are a specialist, strategic partner to global biopharma companies. We provide expertise, derived from our extensive experience, across the drug life cycle.
Science, strategy, and technology underpin our business, but it is driven by deep, collaborative relationships. As true partners, we are focused on helping clients unlock the full potential of their innovations and improve people’s lives.

WHAT ROLE WILL I PLAY ON PROJECTS?

As a Director / Associate Principal, you will act as a strategic partner to our clients, leading high-impact consulting engagements that shape the development and commercialization of biopharmaceutical assets. You will:

• Serve as the primary client advisor, providing strategic recommendations based on deep medical and scientific expertise
• Lead project teams in delivering actionable insights, ensuring that medical and scientific perspectives are integrated into broader commercial and competitive strategies
• Build long-term relationships with clients, identifying opportunities to expand engagements and drive impact across their portfolios
• Oversee multiple projects concurrently, ensuring high-quality execution and delivery
• Contribute to thought leadership by developing industry insights and best practices

DAY-TO-DAY RESPONSIBILITIES

Business Development and Thought Leadership

• Identify opportunities for new consulting engagements within existing and new client accounts
• Author compelling proposals and presentations to win new business
• Contribute to compelling thought leadership (e.g., white papers, conference presentations, industry publications)
• Stay ahead of industry trends, advising clients on emerging opportunities and challenges

Client and Project Leadership

• Lead complex medical and scientific strategy engagements (e.g., clinical trial strategy, medical affairs planning), managing the full project lifecycle from scoping to execution
• Guide teams in conducting rigorous scientific analysis, synthesizing data into actionable recommendations
• Oversee the development of client deliverables, ensuring clarity, impact, and strategic alignment
• Present recommendations to senior client stakeholders with confidence and thought leadership
• Oversee primary and secondary research to inform strategic decision-making
• Manage in-depth analysis of clinical trial landscapes, regulatory pathways, and competitive dynamics
• Pressure-test hypotheses with key stakeholders, including KOLs and industry experts

Team Development and Mentorship

• Lead and mentor a team of consultants and engagement managers, providing coaching and professional development support
• Contribute to internal training initiatives, helping to build capabilities across the Medical and Scientific Strategy practice
• Foster a safe, collaborative, and high-performing team environment, ensuring consistent quality and impact across engagements

WHAT SKILLS AND EXPERIENCE DO I NEED FOR THIS ROLE?

• Advanced degree in life sciences (PhD, MD, PharmD, or equivalent strongly preferred)
• 4+ years of consulting experience within the biopharmaceutical industry, with a focus on medical and scientific strategy
• Strong understanding of drug development across early- and late-stage clinical development, regulatory strategy, and medical affairs
• Expertise in key therapeutic areas such as oncology, immunology, or rare diseases preferred
• Proven ability to lead strategic consulting engagements, including managing client relationships and driving impactful recommendations
• Experience managing teams and mentoring junior consultants in a fast-paced, dynamic environment
• Strong analytical and problem-solving skills, with the ability to synthesize complex scientific data into actionable insights
• Excellent written and verbal communication skills, including experience presenting to senior-level stakeholders