Senior Hematology Clinical Development Director

AbbVie

North Chicago (IL)

On-site

USD 180,000 - 240,000

Full time

2 days ago
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Benefits offered by this job

Paid time off
Medical/dental/vision insurance
401(k)
Long-term incentives

Job summary

AbbVie in North Chicago, IL is seeking an experienced clinical development professional to oversee design, execution, and interpretation of one or more clinical programs, ensuring study integrity and regulatory compliance.

You will lead cross-functional teams, manage timelines and safety data, and contribute to translational strategies and regulatory submissions. Requires MD/DO and 2+ years in clinical trials, with strong English communication in a global, compliant environment.

Qualifications

  • MD/DO or non-US equivalent with relevant therapeutic specialty.
  • At least 2 years of clinical trial experience in pharma, academia, or equivalent.
  • Ability to run a clinical research program with minimal supervision.
  • Strong English oral and written communication skills.

Responsibilities

  • Oversees the direction, planning, execution, and interpretation of clinical trials or research activities.
  • Manages design and implementation of clinical development programs within a Product Development Plan.
  • Oversees study enrollment, timelines, and safety/efficacy data reporting.
  • Contributes to regulatory submissions, protocols, and study documents.
  • Collaborates with Medical Directors, Clinical Scientists, and cross-functional teams.

Skills

Clinical trial leadership
Cross-functional teamwork
Regulatory compliance
English communication

Education

MD/DO or equivalent

Job description

AbbVie in North Chicago, IL is seeking an experienced clinical development professional to oversee design, execution, and interpretation of one or more clinical programs, ensuring study integrity and regulatory compliance.

You will lead cross-functional teams, manage timelines and safety data, and contribute to translational strategies and regulatory submissions. Requires MD/DO and 2+ years in clinical trials, with strong English communication in a global, compliant environment.

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