Clinical Research Supervisor (Oncology)

İnnovex Sağlık Ürünleri Pazarlama Hizm. Ve Danış.

CLINICAL RESEARCH SUPERVISOR (ONCOLOGY)

About Innovex

Innovex provides high-quality solutions to pharmaceutical, biotechnology, and medical device companies through Patient Support Programs, Risk Management Programs, and Contract Sales Teams. As an IQVIA company, Innovex delivers flexible and innovative services that support healthcare organizations in achieving better patient outcomes.

Innovex is an IQVIA company.

We are seeking a highly strategic and dedicated Clinical Research Supervisor (Oncology) to join an exciting clinical research project. In this role, you will lead the core project team, overseeing all aspects of clinical trial execution to ensure alignment with operational goals, timelines, and regulatory standards. You will act as a key liaison across clinical, medical, and operational functions to accelerate study delivery and ensure high-quality outcomes.

Key Responsibilities

• Lead the end-to-end planning, execution, and monitoring of oncology clinical trials.
• Build and guide cross-functional project teams, ensuring effective communication throughout all study phases.
• Monitor study progress against established milestones and proactively manage project risks.
• Drive timely issue resolution and support successful study delivery.
• Ensure compliance with ICH-GCP guidelines, applicable local regulations, and study procedures.
• Manage project financial activities, including budget forecasting, scope management, and resource allocation.
• Collaborate closely with internal and external stakeholders to ensure project objectives are achieved.
• Coordinate and support clinical research activities acrossmultiple countries and international stakeholders.
• Travel as required to support project deliverables, study oversight activities, and stakeholder engagement.

Qualifications & Skills

• Bachelor's degree or higher in Life Sciences, Pharmacy, or a related scientific field.
• Minimum 5 years of hands-on experience in clinical research.
• Proven experience managing oncology clinical trials.
• Strong knowledge of ICH-GCP and clinical research regulations.
• Fluent in English, both written and verbal.
• Demonstrated project management experience with a track record of delivering clinical studies on time and within budget.
• Excellent planning, prioritization, problem-solving, and organizational skills.
• Ability to manage multiple priorities while maintaining a high level of quality and accuracy.
• Experience with complex therapeutics, including monoclonal antibodies and biosimilars, is highly preferred.
• Willingness to travel internationally as required.

Location

Istanbul, Türkiye