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Senior Director, Clinical Program

15+ years
$216,700.00 – $433,300.00
10 March 10, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

 


Senior Director, Clinical Program

Category: Medical and Clinical Affairs

About Abbott:

Abbott is a global healthcare leader dedicated to helping people live healthier lives at all stages. With a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines, Abbott operates in more than 160 countries with a workforce of 114,000 employees.

Why Work at Abbott?

  • Career development opportunities in an international company.
  • Free medical coverage in the Health Investment Plan (HIP) PPO.
  • Excellent retirement savings plan with high employer contribution.
  • Tuition reimbursement and the Freedom 2 Save student debt program.
  • Recognized as a top workplace for diversity, working mothers, female executives, and scientists.

The Opportunity:

This leadership role will oversee Clinical Research professionals, including Clinical Affairs, Clinical Science, Clinical Biometrics (Statistics), Clinical Safety, Clinical Quality, and Clinical Project Management. The position ensures compliance with regulatory requirements, leads clinical research initiatives, and provides strategic guidance to the division.

Key Responsibilities:

  • Ensure compliance with Corporate and Divisional policies and procedures.
  • Provide clinical support to business unit leaders.
  • Represent the division in external interactions with key clinicians and KOLs.
  • Lead and mentor Clinical Research teams worldwide.
  • Develop and implement strategic plans for clinical research functions.
  • Manage cross-functional teams within the Clinical Research organization.
  • Direct clinical study design, development, and monitoring.
  • Lead interactions at trial sites and represent clinical research in business activities.
  • Establish clinical protocols supporting product claims and regulatory submissions.
  • Ensure adherence to ICH/GCP, risk management, and quality guidelines.
  • Review and approve clinical study data for regulatory submissions.
  • Provide compliance guidance and oversee audits of clinical research.
  • Represent the division at regulatory meetings and trade events.

Qualifications:

  • Education: Bachelor's Degree required; Master's Degree preferred.
  • Experience: Minimum 15 years of relevant experience.
  • Strong expertise in both scientific and business aspects of clinical research.
  • Thorough understanding of the scientific method for clinical evaluations.

Compensation:

  • Base salary: $216,700 – $433,300 (Pay may vary by location).

How to Apply:

Learn more about Abbott’s health and wellness benefits: www.abbottbenefits.com

Abbott is an Equal Opportunity Employer committed to employee diversity.

Connect with Abbott: