Astek Middle East

1 Job

77 Employees

About the Company

Astek Middle East offers to provide IT services throughout the Middle East region including Saudi Arabia, UAE and Jordan in the following sectors : - Public & Government - Healthcare - Airlines & Tourism Industries - Transportation - Retail - Banking You can reach us at contact-astekme@astek-international.com More information at https://astekgroup.fr/country/saudi-arabia/?lang=en and https://astekgroup.fr/country/united-arab-emirates/?lang=en Founded in France in 1988, Astek is a global player in engineering and technology consulting, present on five continents. With its expertise in many industrial and tertiary sectors, it supports its international clients in the intelligent deployment of their products and services, and in the implementation of their digital transformation. Since its creation, the Group has based its development on a strong culture of entrepreneurship and innovation, and on the support and skills development of its 10,000 employees who are committed every day to promoting combination of digital technologies and complex systems engineering. The Group had a turnover of €620 million in 2023. Contact us: contact-astekme@astek-international.com

Listed Jobs

Company Name: Astek Middle East
Job Title: Clinical Project Manager &#8211; Montréal, Canada (F/M)
Job Description: **Job title** Clinical Project Manager **Role Summary** Lead end‑to‑end management of Phase I/II immuno‑oncology clinical trials, ensuring timely delivery, regulatory compliance, risk mitigation, and high data integrity. **Expectations** Deliver projects on schedule and within budget while maintaining GCP standards; mentor cross‑functional teams; cultivate strong sponsor and regulatory relationships; continuously improve operational processes. **Key Responsibilities** - Design and execute trial master plans, study protocols, ICFs, and eCRFs. - Identify, assess, and mitigate risks; enforce ICH GCP and regulatory guidelines. - Lead and train clinical research associates and documentation specialists. - Manage vendor contracts, budgets, and performance; act as primary vendor liaison. - Prepare and review project documents, budgets, vendor contracts, and annual reports. - Facilitate clear communication among sponsors, regulatory authorities, and internal teams. - Analyze and summarize data for regulatory submissions and reporting. **Required Skills** - 5–8 years clinical operations experience, including Phase I/II trials in immuno‑oncology. - Deep knowledge of ICH GCP and related legislation. - Proficiency with eCRF databases and clinical trial management systems. - Strong project, risk, vendor, and budget management abilities. - Excellent written and verbal communication. - Organizational, pragmatic, flexible, persistent, and results‑oriented leadership. **Required Education & Certifications** - Master’s degree in Biology, Biomedical Sciences, Pharmacy, or equivalent. - Certification in Clinical Research (e.g., CCRA, Certified Clinical Research Professional) preferred.