Global Clinical Research Associate — Trials & Compliance

Ctifacts; Riyadh; On-site; SAR 180,000 - 240,000; Full time

Job summary

CTI Clinical Trial and Consulting Services in Riyadh, Saudi Arabia, seeks a Clinical Research Associate to support successful conduct of trials and act as the main site contact for CTI.

Responsibilities include performing initiation, monitoring and close-out visits, supporting regulatory start-up activities, ensuring data integrity and timelines, and participating in global project meetings; requires 2–3 years of CRA experience and strong ICH-GCP knowledge.

Qualifications

• 2–3 years of clinical research experience as a CRA or related profession.
• Life science background.
• Excellent knowledge of ICH-GCP and regulatory requirements.

Responsibilities

• Conduct evaluation, initiation, monitoring and close out visits.
• Assist with regulatory and study start-up activities including contract and budget negotiations.
• Ensure clinical data integrity and meet study timelines.
• Provide ongoing updates and support to project management.
• Attend global project meetings including investigator meetings and global team teleconferences.
• Complete assigned training programs in drug development processes, therapeutic areas, GCPs and any applicable local regulatory requirements.

Skills

CRA experience

Life science background

ICH-GCP knowledge

Job description

CTI Clinical Trial and Consulting Services in Riyadh, Saudi Arabia, seeks a Clinical Research Associate to support successful conduct of trials and act as the main site contact for CTI.

Responsibilities include performing initiation, monitoring and close-out visits, supporting regulatory start-up activities, ensuring data integrity and timelines, and participating in global project meetings; requires 2–3 years of CRA experience and strong ICH-GCP knowledge.