Evidence Generation Lead: Studies & Publications

BioSpace; Riyadh; On-site; SAR 180,000 - 260,000; Full time

Job summary

AbbVie seeks a qualified Evidence Generation Specialist/Advisor to lead end-to-end evidence-generation studies and scientific publications. You will coordinate CROs, vendors, investigators, timelines, and budgets while ensuring publication planning and dissemination across Medical, Market Access, and Regulatory teams.

You will collaborate with Medical Operations, Finance, Legal, and Clinical Operations to ensure compliant study delivery, audit readiness, and timely reporting of study health.

Qualifications

• Bachelor’s degree in Medicine, Pharmacy, Life Sciences, Public Health, Healthcare Sciences, or related field.
• Advanced degree (Master’s) in Clinical Research, Epidemiology, Public Health, Health Economics, or related field is a plus.
• Minimum 3 years of experience in Clinical Research Operations and/or Evidence Generation.

Responsibilities

• Lead end-to-end execution of approved evidence-generation studies and publications.
• Manage CROs, vendors, investigators, timelines, budgets, and dissemination activities.
• Coordinate site/investigator engagement, start-up activities, and close-out processes.
• Monitor recruitment, progress, risks, and monthly health updates for studies.
• Own publication planning and manuscript/abstract development and submission.

Skills

Project management

Organizational skills

Stakeholder management

Study management

Analytical skills

Bilingual English/Arabic

Education

Bachelor’s degree in Medicine/Pharmacy/Life Sciences

Master’s degree in Clinical Research/Public Health

Tools

MS Office

Project tracking tools

Job description

AbbVie seeks a qualified Evidence Generation Specialist/Advisor to lead end-to-end evidence-generation studies and scientific publications. You will coordinate CROs, vendors, investigators, timelines, and budgets while ensuring publication planning and dissemination across Medical, Market Access, and Regulatory teams.

You will collaborate with Medical Operations, Finance, Legal, and Clinical Operations to ensure compliant study delivery, audit readiness, and timely reporting of study health.