Oncology Clinical Development Director

Regulatory Jobs; Chicago (IL); In loco; USD 120.000 - 180.000; Tempo pieno

Vantaggi offerti da questo lavoro

Long-term incentive programs

Comprehensive benefits package

Descrizione del lavoro

AbbVie is seeking a clinician-scientist to oversee clinical development programs in the US. The role emphasizes protocol design, study execution, and collaboration with medical affairs and regulatory teams.

The candidate will ensure adherence to Good Clinical Practices and contribute to scientific content for regulatory submissions. Residency and optional subspecialty training are valued, with strong English communication required.

Competenze

• MD/DO or non-US equivalent required or strongly preferred.
• Residency program completion strongly preferred.
• Experience with clinical trials and regulatory/compliance is desirable.

Mansioni

• Design and implement study protocols for a clinical development program.
• Oversee study enrollment, timelines, and safety/efficacy data.
• Contribute to protocol design, analysis, and regulatory submissions.
• Collaborate with Clinical Strategy Team and cross-functional partners.

Conoscenze

Cross-functional collaboration

Clinical trial experience

Strong English communication

Formazione

MD/DO or non-US equivalent

Residency completed

Fellowship desirable

Descrizione del lavoro

AbbVie is seeking a clinician-scientist to oversee clinical development programs in the US. The role emphasizes protocol design, study execution, and collaboration with medical affairs and regulatory teams.

The candidate will ensure adherence to Good Clinical Practices and contribute to scientific content for regulatory submissions. Residency and optional subspecialty training are valued, with strong English communication required.