PI Fieldwork Support

PI Fieldwork Support – Drive Impactful Clinical Research in Riyadh

At IQVIA, we are committed to advancing global health through innovative clinical research solutions. As a **PI Fieldwork Support Specialist**, you will play a pivotal role in ensuring the seamless execution of clinical trials, bridging the gap between investigators and field operations. This dynamic position offers an opportunity to contribute to groundbreaking research while developing expertise in regulatory compliance, data integrity, and patient-centric fieldwork strategies.

In this full-time role based in **Riyadh**, you will collaborate with cross-functional teams to optimize trial workflows, enhance investigator engagement, and uphold the highest standards of ethical conduct and data accuracy. Your work will directly impact the success of clinical studies, driving meaningful advancements in healthcare outcomes.

Key Responsibilities:

Your role will encompass a diverse range of responsibilities, including:

• Investigator Support: Act as a liaison between Principal Investigators (PIs) and IQVIA’s fieldwork teams to ensure alignment on trial objectives, timelines, and resource allocation. Provide proactive guidance to streamline site operations and mitigate potential challenges.
• Fieldwork Coordination: Assist in planning and executing on-site visits, ensuring adherence to protocols, regulatory requirements, and IQVIA’s operational standards. Monitor trial progress and escalate issues promptly to maintain trial integrity.
• Data Integrity & Compliance: Collaborate with data management teams to verify source data accuracy and ensure compliance with ICH-GCP guidelines and local regulatory bodies. Contribute to audit readiness by maintaining thorough documentation and transparency.
• Training & Capacity Building: Support the training of site personnel and investigators on best practices in clinical research, including protocol adherence, patient recruitment, and data collection methodologies.
• Stakeholder Engagement: Foster strong relationships with PIs, site staff, and internal teams to foster a collaborative environment. Act as a trusted advisor, providing insights to enhance trial efficiency and participant experience.
• Reporting & Analytics: Compile and analyze fieldwork metrics to identify trends, bottlenecks, or areas for process improvement. Present actionable recommendations to leadership for continuous optimization.

Why Join IQVIA?

IQVIA is a leader in clinical research services, empowering organizations to deliver life-changing therapies to patients worldwide. By joining our team in Riyadh, you will:

• Contribute to high-impact clinical trials that shape the future of medicine.
• Develop expertise in regulatory environments, data management, and global clinical operations.
• Work in a collaborative, mission-driven culture that values innovation and excellence.
• Access professional growth opportunities through training, mentorship, and exposure to diverse projects.
• Be part of a dynamic team that prioritizes integrity, accountability, and patient-centered care.

Qualifications & Requirements:

To excel in this role, you should possess:

• A bachelor’s degree in a relevant field such as Health Sciences, Pharmacy, Life Sciences, or a related discipline. Advanced degrees or certifications in clinical research (e.g., Certified Clinical Research Coordinator (CCRC)) are a plus.
• Proven experience in clinical research support, site coordination, or fieldwork operations, preferably in a regulatory environment. Familiarity with ICH-GCP guidelines is essential.
• Strong analytical and problem-solving skills with the ability to interpret complex trial data and regulatory requirements.
• Excellent communication and interpersonal abilities to engage effectively with investigators, site staff, and cross-functional teams.
• Fluency in Arabic and English is required, with advanced proficiency in both written and spoken communication.
• Familiarity with electronic data capture (EDC) systems, CRM tools, and clinical trial management software is advantageous.
• A results-driven mindset with a commitment to ethical standards and continuous improvement.

IQVIA is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

Ready to make a difference in clinical research? Join our team in Riyadh and be part of a global movement transforming healthcare for the better.