Scientific Director Pharmacology

7 days ago

Bengaluru, Karnataka, India Net Connect Full time ₹ 15,00,000 - ₹ 20,00,000 per year

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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