Senior Clinical Development Leader

BioSpace; North Chicago (IL); On-site; USD 180,000 - 260,000; Full time

Job summary

AbbVie is seeking an MD/DO or equivalent to lead clinical development efforts across one or more programs, guiding study design, data interpretation, and regulatory submissions. The role requires collaboration with cross-functional teams to advance scientific and business strategy while ensuring compliance with GCP and regulatory standards.

The candidate should have at least 2 years of clinical trial experience and strong English communication skills, with a preference for experience in

Qualifications

• MD/DO or non-US equivalent with relevant therapeutic specialty.
• Residency completion strongly preferred; subspecialty fellowship desirable.
• At least 2 years of clinical trial experience in pharma, academia, or equivalent.
• Experience with psychedelic drug development highly preferred.
• Ability to run a clinical research program of moderate complexity with minimal supervision.
• Ability to work cross-functionally in a global team.
• Knowledge of clinical trial methodology and regulatory requirements.
• Excellent oral and written English communication skills.

Responsibilities

• Design and implement one or more clinical development programs within an overall Product Development Plan.
• Oversee study enrollment and timelines; monitor study integrity and safety/efficacy data.
• Prepare and report protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions.
• Serve as clinical expert and coordinate activities with internal stakeholders.
• May chair an Integrated Evidence Strategy Team (IEST) and supervise matrix team members.
• Engage with external stakeholders and participate in translational strategy development.
• Stay current on regulatory requirements and Good Clinical Practices.

Skills

Clinical trial management

Cross-functional teamwork

Regulatory knowledge

English proficiency

Education

Medical degree (MD/DO)

Job description

AbbVie is seeking an MD/DO or equivalent to lead clinical development efforts across one or more programs, guiding study design, data interpretation, and regulatory submissions. The role requires collaboration with cross-functional teams to advance scientific and business strategy while ensuring compliance with GCP and regulatory standards.

The candidate should have at least 2 years of clinical trial experience and strong English communication skills, with a preference for experience in