Instagram
youtube
Facebook

Edqy-0, Scientific Director Of Clinical Pharmacology

7+ years years
Not Disclosed
10 Aug. 30, 2025
Job Description
Job Type: Full Time Education: Doctoral degree (PhD, PharmD, or MD) Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

πŸ§ͺ Job Title:

Scientific Director, Clinical Pharmacology

πŸ†” Job ID:

290141

πŸ“ Location:

Hyderabad, Andhra Pradesh, India

πŸ•’ Job Type:

Full-time


🌍 About Merck:

At Merck, we are united by curiosity and a passion for improving lives through science and technology. In our Healthcare division, we aim to help create, improve, and prolong lives through innovative medicines, devices, and technologies, with a global reach across Oncology, Neurology, and Fertility.

We're committed to fostering an inclusive, flexible, and growth-oriented culture across our global teams.


🎯 Role Overview:

The Scientific Director, Clinical Pharmacology is a key strategic and scientific leader within the Quantitative Pharmacology function, part of the Clinical Measurement Sciences (CMS) organization. You will lead the Clinical Pharmacology (CP) Expert Team, responsible for developing and executing clinical pharmacology and Model Informed Drug Development (MIDD) strategies from early clinical stages through late-stage development and lifecycle management.

You’ll collaborate cross-functionally with stakeholders from Clinical Development, Biostatistics, Pharmacokinetics, Biomarkers, Research, and Regulatory Affairs.


πŸ“Œ Key Responsibilities:

πŸ”Ή Clinical Pharmacology Strategy:

  • Lead development and execution of Clinical Pharmacology (CP) strategies aligned with clinical development plans.

  • Ensure CP strategies are tailored to indication, patient population, phase, and competitive landscape.

πŸ”Ή Scientific & Technical Expertise:

  • Serve as the scientific lead and expert in PK, PK/PD, ADME, and posology.

  • Make strategic decisions related to:

    • Dose selection and optimization (from FIH through post-marketing)

    • Exposure–response analysis

    • QTc and immunogenicity assessments

  • Oversee PK/PD data analysis, interpretation, and documentation.

πŸ”Ή Regulatory Documentation:

  • Lead preparation of CP-related sections in documents such as:

    • Clinical protocols

    • Investigator Brochures (IBs)

    • IND/IMPDs

    • CTDs

    • NDAs and briefing books

πŸ”Ή Collaboration & Representation:

  • Represent Clinical Pharmacology at global cross-functional project teams.

  • Promote Model Informed Drug Development (MIDD) strategies across internal and external stakeholders.

  • Participate in due diligence activities when needed.


πŸ‘€ Candidate Profile:

πŸŽ“ Education & Languages:

  • Doctoral degree (PhD, PharmD, or MD) in clinical pharmacology, pharmacometrics, pharmaceutical sciences, engineering, statistics, or a related discipline.

  • Fluency in English (written and spoken).

πŸ’Ό Professional Experience:

  • 7+ years of experience in the pharmaceutical industry or postdoctoral training with direct exposure to clinical drug development.

  • Proven leadership in cross-functional environments and matrix organizations.

πŸ›  Technical Expertise:

  • In-depth understanding of:

    • Clinical pharmacology, including PK, ADME, posology

    • Quantitative translational sciences

    • Regulatory requirements for submissions (FDA, EMA, etc.)

  • Familiarity with oncology, immunology, or immuno-oncology is a plus.

  • Hands-on experience with PK/PD modeling and MIDD approaches is beneficial.

🀝 Soft Skills & Competencies:

  • Strong interpersonal and communication skills.

  • Ability to prioritize, manage multiple projects, and adapt to changing business needs.

  • Collaborative, strategic thinker with team-building capabilities.

  • Effective communicator with the ability to translate complex data into meaningful recommendations.


πŸ’Ό What We Offer:

At Merck, we are committed to your growth and wellbeing. Our benefits support personal and professional development, physical and mental health, family needs, and lifestyle flexibility.

πŸ’° Financial & Protection:

  • Programs for long-term financial security for you and your family.

🧠 Health & Wellbeing:

  • Comprehensive health check-ups, medical coverage, and wellness programs.

πŸ‘¨‍πŸ‘©‍πŸ‘§‍πŸ‘¦ Family:

  • Support through fertility benefits and assistance for all stages of family life.

🌴 Time Off:

  • Generous paid leave options and specific leave types for life events.

🧘‍♀️ Lifestyle:

  • Flexible work options, access to gyms, car programs, and discounts.


πŸ” Recruitment Process:

  1. Apply: Submit your application online for suitable openings.

  2. Screen: Applications are reviewed for alignment with job criteria.

  3. Assess: Selected candidates proceed to phone, video, or face-to-face interviews.

  4. Mutual Agreement: If selected, Merck extends an offer.

  5. Onboarding: A structured process ensures a smooth start in your new role.


⚠️ Notice on Fraudulent Job Offers:

Be cautious of fake job offers misrepresenting Merck. All official communication is handled via verified Merck channels. Please refer to the fraud alert section on our official careers page for more information.


βœ… Apply Now:

Become part of Merck’s mission to spark discovery and elevate humanity. Help shape the future of clinical development with cutting-edge science and data-driven decision-making.