Senior Director, Hematology Clinical Development

AbbVie

Florham Park (NJ)

On-site

USD 180,000 - 240,000

Full time

2 days ago
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Benefits offered by this job

Medical/dental/vision insurance
Paid time off
401(k)

Job summary

AbbVie is seeking a leader to oversee direction, planning, execution, and interpretation of clinical trials within one or more development programs, contributing to product strategy and scientific objectives. You will collaborate with cross-functional teams to drive high-quality data and strategic decisions.

You will work with investigators and study staff, ensure study integrity and timelines, and contribute to regulatory submissions and publications.

Qualifications

  • Must possess excellent oral and written English communication skills.
  • Ability to run a clinical research program of moderate complexity with minimal supervision.
  • Ability to interact externally and internally to support a global scientific and business strategy.

Responsibilities

  • Oversees design and execution of one or more clinical development programs.
  • Monitors study integrity and data on safety and efficacy of the molecule.
  • Oversees enrollment timelines and overall timelines for key deliverables.
  • Provides in-house clinical expertise and coordinates translational strategies with internal stakeholders.
  • Participates in due diligence or other business development activity as needed.
  • Ensures adherence to Good Clinical Practices and regulatory compliance.

Skills

English communication
Program management
Stakeholder management

Education

MD/DO degree or equivalent

Job description

AbbVie is seeking a leader to oversee direction, planning, execution, and interpretation of clinical trials within one or more development programs, contributing to product strategy and scientific objectives. You will collaborate with cross-functional teams to drive high-quality data and strategic decisions.

You will work with investigators and study staff, ensure study integrity and timelines, and contribute to regulatory submissions and publications.

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