Director, Clinical Science & PK Strategy

Abbott Laboratories

Hinoba-an

On-site

PHP 1,800,000 - 3,000,000

Full time

10 days ago
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Job summary

Abbott Laboratories is seeking a Clinical Sciences Director to lead the Clinical Pharmacology and Bioanalytics teams, setting strategic direction for global and regional clinical development in alignment with EPD objectives. You will oversee budgets, resources, and governance across studies, ensuring scientific excellence and regulatory compliance.

The role requires MD/PhD or equivalent with 10–15 years in the pharmaceutical industry, strong leadership, and experience guiding CROs and external

Qualifications

  • Demonstrated ability to lead and guide teams in multi country complex organization.
  • 10-15 years of experience in pharmaceutical industry with strong understanding of formulation development programs and guidance of targeted product profile, differentiated generics industry and biosimilar/biologic experience on clinical programs.
  • Understanding and knowledge of various CROs in EM.

Responsibilities

  • Serves as a core member of Clinical development leadership Team and helps set strategic direction for Global and regional clinical development functions.
  • Accountable for allocation of clinical pharmacology and bioanalytic team and budgets to project teams to meet study timelines and ensure data quality.
  • Guides the team on pharmacology and formulation guidance, liaises with CROs, RA, and other stakeholders to support product success.

Skills

Communication
Leadership
Decision Making
Strategic thinking
Coaching and Consulting
Cross-Team Integration
Planning & Organizing
Stakeholder management
Customer Service Orientation

Education

MD/ PhD or equivalent

Job description

Abbott Laboratories is seeking a Clinical Sciences Director to lead the Clinical Pharmacology and Bioanalytics teams, setting strategic direction for global and regional clinical development in alignment with EPD objectives. You will oversee budgets, resources, and governance across studies, ensuring scientific excellence and regulatory compliance.

The role requires MD/PhD or equivalent with 10–15 years in the pharmaceutical industry, strong leadership, and experience guiding CROs and external

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