Manager, Aesthetics Clinical Development
AbbVie
August 14, 2026
On-site
Irvine, CA
$109,500 - $208,500 USD yearly
Clinical Research and Development
Responsibilities:
- Prepare scientific reports/presentations for clinical trials using software/templates; review/contribute to clinical protocols and assist in data interpretation.
- Coordinate advisory meeting agendas, activities, slide decks, and consulting agreements.
- Follow IQS procedures, study protocols, and management directives for clinical studies.
- Lead study development using current electronic document conventions/processes to ensure scientific integrity.
- Receive/complete tasks from function/Therapeutic Area MD/Scientific Staff within timelines with minimal supervision.
- Participate in process improvement initiatives; review decisions impacting project timelines.
- Analyze clinical study data (including statistical data) to support ongoing blinded/unblinded PK, safety, and efficacy reviews.
- Perform literature/competitive intelligence searches to resolve scientific/technical issues.
- Provide key clinical study information to function/therapeutic area and management.
- May lead teams and supervise/mentor direct reports.
Qualifications:
- Bachelor’s/Master’s in science (11+ years pharmaceutical industry) or Pharm-D/PhD with 1+ year.
- Ability to understand complex clinical study principles.
- Advanced ability with technology to analyze data and create reports/presentations/posters/manuscripts.
- Experience in team/drug development/scientific project leadership.
- Experience supporting clinical research/drug development/therapeutic area operations.
- Proven successful projects; in-depth knowledge of clinical study issues.
- Resourcefulness, attention to detail, and strong oral/written communication.
Benefits (as stated): paid time off; medical/dental/vision insurance; 401(k); short-term and long-term incentive eligibility.
Location: Onsite in Irvine, CA.
- Prepare scientific reports/presentations for clinical trials using software/templates; review/contribute to clinical protocols and assist in data interpretation.
- Coordinate advisory meeting agendas, activities, slide decks, and consulting agreements.
- Follow IQS procedures, study protocols, and management directives for clinical studies.
- Lead study development using current electronic document conventions/processes to ensure scientific integrity.
- Receive/complete tasks from function/Therapeutic Area MD/Scientific Staff within timelines with minimal supervision.
- Participate in process improvement initiatives; review decisions impacting project timelines.
- Analyze clinical study data (including statistical data) to support ongoing blinded/unblinded PK, safety, and efficacy reviews.
- Perform literature/competitive intelligence searches to resolve scientific/technical issues.
- Provide key clinical study information to function/therapeutic area and management.
- May lead teams and supervise/mentor direct reports.
Qualifications:
- Bachelor’s/Master’s in science (11+ years pharmaceutical industry) or Pharm-D/PhD with 1+ year.
- Ability to understand complex clinical study principles.
- Advanced ability with technology to analyze data and create reports/presentations/posters/manuscripts.
- Experience in team/drug development/scientific project leadership.
- Experience supporting clinical research/drug development/therapeutic area operations.
- Proven successful projects; in-depth knowledge of clinical study issues.
- Resourcefulness, attention to detail, and strong oral/written communication.
Benefits (as stated): paid time off; medical/dental/vision insurance; 401(k); short-term and long-term incentive eligibility.
Location: Onsite in Irvine, CA.