Scientific Director Pharmacology Net Connect

6.0 - 9.0 years

15 - 30 Lacs

bengaluru

Work from Office

Location: Bangalore Experience: 6 - 9 Years CTC: 10 - 30 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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