Key Responsibilities:
- Study-level oversight and leadership of global trials, including vendor management, recruitment, and meeting facilitation.
- Develop and manage study materials like protocols, budgets, and regulatory submissions.
- Ensure inspection readiness and manage risk identification and mitigation.
Qualifications:
- Bachelor's Degree with at least 4 years of progressive pharma or clinical research experience.
- Proficiency in EDC, IRT, CTMS, and eTMF systems.
- Strong analytical, organizational, and interpersonal skills with a proactive, collaborative mindset.
Preferred Experience:
- Exposure to study initiation through completion activities and global study exposure.
- Competent in applying standard quality procedures (SOP, ICH/GCP, Global Regulations).
Abbvie
AbbVie discovers and delivers innovative medicines and solutions to address serious health issues in immunology, oncology, neuroscience, and aesthetics. As a global biopharmaceutical company with a robust pipeline, they emphasize integrity and innovation, serving patients worldwide with a dedicated team.