• Proven track record to attain and maintain a good solid understanding of ICH GCP, applicable regulations and Company/Client procedural documents
• Solid understanding in all phases of clinical trials, specifically study startup, study maintenance and study close out
• Skilled in handling, engaging, motivating, mentoring and retaining staff
• Knowledge of budgets, projects and metrics (financial and eye for business)
• Ability to balance multiple tasks simultaneously, to meet meticulous timelines and to work optimally in stressful situations
• Strong interpersonal skills and strong attention to detail
• Strong interpersonal skills both written and verbal, including significant command of English; and excellent interpersonal and conflict resolution skills
These cookies are necessary for the website to function and cannot be turned off in our systems. You can set your browser to block these cookies, but then some parts of the website might not work.
Security
User experience
Target group oriented cookies
These cookies are set through our website by our advertising partners. They may be used by these companies to profile your interests and show you relevant advertising elsewhere.
Google Analytics
Google Ads
We use cookies
🍪
Our website uses cookies and similar technologies to personalize content, optimize the user experience and to indvidualize and evaluate advertising. By clicking Okay or activating an option in the cookie settings, you agree to this.
The best remote jobs via email
Join 5'000+ people getting weekly alerts with remote jobs!