Executive Medical Director, Clinical Strategy & Trials

AbbVie

Illinois

In loco

USD 180.000 - 240.000

Tempo pieno

9 giorni fa

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Paid time off
Medical/dental/vision insurance
401(k) plan
Long-term incentive programs

Descrizione del lavoro

AbbVie is seeking a clinician with leadership in clinical development to steer major programs across the product lifecycle. The role requires coordinating cross-functional teams, ensuring study integrity, and delivering robust data for regulatory submissions.

The candidate will oversee design and reporting of study protocols, safety analyses, and regulatory communications, while staying current with regulatory expectations and industry best practices.

Competenze

  • MD or DO degree with relevant therapeutic specialty; residency preferred.
  • 5–7 years of clinical trial experience in pharma, academia, or equivalent.
  • Ability to run a complex clinical research program independently.
  • Proven leadership skills and ability to lead cross-functional global teams.

Mansioni

  • Lead design, execution, and interpretation of multiple clinical development programs.
  • Oversee study teams, monitor study integrity, and report safety/efficacy data.
  • Lead preparation of protocols, Investigator Brochures, Clinical Study Reports, and regulatory submissions.
  • Serve on Clinical Strategy Teams and coordinate cross-functional Clinical Development Plans.

Conoscenze

Clinical trial leadership
Regulatory compliance knowledge
English communication
Cross-functional teamwork

Formazione

MD/DO (or non-US equivalent)

Descrizione del lavoro

AbbVie is seeking a clinician with leadership in clinical development to steer major programs across the product lifecycle. The role requires coordinating cross-functional teams, ensuring study integrity, and delivering robust data for regulatory submissions.

The candidate will oversee design and reporting of study protocols, safety analyses, and regulatory communications, while staying current with regulatory expectations and industry best practices.

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