Strategic Neuroscience Clinical Development Director

AbbVie Inc.

North Chicago (IL)

On-site

USD 180,000 - 280,000

Full time

4 days ago
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Benefits offered by this job

Long-term incentive programs
Medical/dental/vision insurance
401(k)

Job summary

AbbVie Inc. is seeking an experienced clinical development leader to oversee the direction, planning, and interpretation of one or more clinical programs.

The role combines medical insight with regulatory and compliance expertise to support product strategy across immunology, oncology, and neuroscience. You will manage studies, ensure data integrity, and coordinate protocols, investigator materials, and regulatory submissions while guiding a cross-functional team of Medical Directors and

Qualifications

  • MD/DO or non-US equivalent with relevant specialty; residency preferred.
  • At least 2 years of clinical trial experience in pharma/academia.
  • Experience with psychedelic drug development highly preferred.
  • Ability to run a clinical research program of moderate complexity with minimal supervision.

Responsibilities

  • Oversees design and implementation of one or more clinical development programs.
  • Ensures study integrity and timelines; reviews safety/efficacy data.
  • Coordinates scientific content of protocols and regulatory documents.
  • Mentors Medical Directors and Clinical Scientists as needed.
  • Collaborates with internal stakeholders and external partners.

Skills

Clinical trial management
Regulatory compliance
English communication

Education

MD/DO or non-US equivalent
Residency program
Subspecialty fellowship desirable

Job description

AbbVie Inc. is seeking an experienced clinical development leader to oversee the direction, planning, and interpretation of one or more clinical programs.

The role combines medical insight with regulatory and compliance expertise to support product strategy across immunology, oncology, and neuroscience. You will manage studies, ensure data integrity, and coordinate protocols, investigator materials, and regulatory submissions while guiding a cross-functional team of Medical Directors and

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