Clinical Research Supervisor (Oncology)

Abdi İbrahim, founded in 1912, has the largest product portfolio in the sector and is the largest employer in the Turkish pharmaceutical industry with 5,500 employees. The company has been the leader of Turkey’s pharmaceutical industry since 2002, driven by its strong vision and sustainable growth strategy. Today, Abdi İbrahim operates in 17 countries outside Türkiye and exports to more than 70 countries, ranging from Canada to European Union member states, and from North Africa to Asia. As a corporate citizen committed to creating a better world and a better future, Abdi İbrahim integrates sustainability into all its business processes.Beyond maintaining its position as the leading local pharmaceutical company, the company’s vision is to become one of the top 100 pharmaceutical companies in the world. We are currently looking for a Clinical Research Supervisor t o join our team. Key Responsibilities: Lead the end-to-end planning, execution, and continuous monitoring of complex oncology clinical trials, optimizing for speed, quality, and cost-effectiveness. Build and guide cross‑functional project teams, ensuring effective communication across all phases. Ensure that the legal team is added to the review process for all trial agreements and vendor contracts. Monitor study progress against established milestones, proactively manage risks, and drive timely issue resolution. Ensure strict adherence to ICH GCP guidelines, applicable local regulations, and standard operating procedures (SOPs). Manage project financials, including budget forecasting, scope management, and clinical resource allocation. Qualifications & Skills: Minimum of 5 years of hands-on experience in the clinical research field. Fluent in English (both written and verbal) is essential for seamless global stakeholder communication and clinical documentation. Proven experience managing oncology clinical trials. Familiarity with complex therapeutics, such as monoclonal antibodies and biosimilars, is highly preferred. Strong project management capabilities with a demonstrated track record of successfully delivering clinical studies on time and within budget. Bachelor’s degree or higher in Life Sciences, Pharmacy, or a related scientific field. Excellent problem‑solving, planning, and prioritization skills, with the ability to manage conflicting priorities while maintaining accuracy and quality.