Fadime Acar Ural

Accomplished professional expertise in audit competency and advanced clinical training, demonstrating exceptional skills in quality assurance auditing and clinical leadership. Proven track record in staff training, conflict management and performance management, ensuring effective workload prioritization and procedure development. Adept at patient record auditing with a focus on communication clarity.

Proactivity and stress resilience. Committed to fostering cultural awareness and excelling in project management to drive organizational success. Offering strong foundation in leadership and healthcare management, with focus on team coordination and patients care.

Knowledgeable about implementing clinical protocols and improving driving quality. Ready to use and develop leadership, communication and organizational skills in Clinical Management role.

Senior Clinical Lead - IQVIA - Istanbul Turkey

(2010-06)

• Demonstrated strong leadership throughout the clinical trial process to guide team towards successful outcomes.
• Achieved high level of staff motivation through effective leadership and communication.
• Led training programs to enhance the clinical skills of junior team members.
• Promoted a culture of continuous learning amongst staff members, fostering professional growth and development.
• Adhered strictly to regulatory guidelines during all clinical procedures for compliance assurance.
• Facilitated communication with sponsors to align performance expectations throughout the clinical trials.
• Developed detailed guidelines to establish expected performance standards and procedures for the study.
• Improved quality standards with thorough audit processes and performance reviews.
• Recognized and managed workplace risks, immediately determining best methods for resolution.
• Assisted in recruitment processes to ensure competent clinical staff.
• Fostered a positive work environment through transparent communication and fair decision-making processes.

Clinical Research Associate - Lundbeck Pharma - Istanbul Turkey

(2005-08 - 2010-05)

• Implemented protocols to streamline clinical study processes.
• Maintained confidentiality of subject records, always upholding ethical standards.
• Validated case report forms to ensure accurate data collection and reporting.
• Trained junior staff members, facilitating their professional development.
• Monitored study performance metrics to confirm compliance with study protocols.

Bachelor of Science - Molecular Biology and Genetics - Haliç University (2000-09 - 2005-01)