
Scientific Director Pharmacology
6 days ago
Location: Bangalore
Experience: 6 - 9 Years
CTC: LPA
Notice Period: Immediate to 15 Days
About the Role
We are seeking a Scientific Director Pharmacology to lead our clinical pharmacology strategy and execution in drug development. In this pivotal role, you will drive Model Informed Drug Development (MIDD), influence cross-functional strategies, and deliver impactful pharmacology solutions that accelerate drug discovery and clinical outcomes. You will collaborate with global stakeholders, lead expert teams, and ensure high-quality regulatory submissions while contributing to cutting-edge healthcare innovations.
This role offers an opportunity to make a direct impact on patient outcomes, stay at the forefront of scientific research, and grow your career in a collaborative and innovation-driven environment.
Key Responsibilities
- Lead the Clinical Pharmacology (CP) Expert Team in developing and executing strategies from early through late-stage clinical development.
- Design and deliver MIDD strategies that optimize dosing, PK/PD modeling, and translational sciences.
- Partner with pharmacometrics, biostatistics, and other functions to ensure robust PK/PD analysis, interpretation, and reporting.
- Provide scientific expertise on dose selection, study design, and clinical pharmacology approaches across phases.
- Contribute to and review regulatory documents such as clinical protocols, INDs, NDAs, IBs, CTDs, briefing books, and due diligence reports.
- Represent clinical pharmacology in cross-functional meetings and external regulatory interactions.
- Monitor competitive landscape and industry trends to align strategies with evolving regulatory and scientific expectations.
- Promote collaboration in an international, matrix-driven environment, mentoring team members and driving operational excellence.
Ideal Candidate Profile
- 6–9 years of experience in pharmaceutical/biotech industry or postdoctoral research with direct clinical drug development experience.
- Doctorate degree (PhD, PharmD, or MD) in Clinical Pharmacology, Pharmaceutics, Pharmacokinetics, Pharmacology, Pharmacometric Sciences, Statistics, or related disciplines.
- Strong expertise in PK, PD, ADME, and quantitative translational sciences.
- In-depth knowledge of regulatory requirements and submissions across global regions.
- Proven experience in MIDD strategy design and execution.
- Understanding of oncology, immunology, and/or immuno-oncology is preferred.
- Hands-on experience with modeling and simulation tools is an advantage.
- Strong communication, presentation, and stakeholder management skills.
- Ability to manage multiple priorities in a fast-paced, global matrix environment.
Why Join Us?
At NCG (NetConnect Global), we partner with global enterprises and healthcare leaders to build future-ready solutions. Since 1997, we have been empowering businesses with digital transformation, AI/ML, advanced analytics, cybersecurity, and cloud solutions.
We are Great Place to Work Certified, backed by a diverse team of 2,000+ professionals worldwide.
Benefits you'll enjoy:
- Family First: 6 months paid maternity leave, 5 days paid paternity leave.
- Health & Wellness: Comprehensive group medical insurance with family coverage.
- Financial Security: Accident insurance (2x salary), gratuity, ESIC benefits.
- Employee Support: Confidential counseling & wellness programs.
- Career Growth: Exposure to global healthcare projects, regulatory strategy, and scientific leadership
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