Site Start-Up Specialist in Clinical Research (Bucharest)

The successful candidate will hold
• educational background in disciplines of science or medicine/health care
• excellent communication skills in the local language as well as in English are essential
• good computer skills
• excellent self-organisation
• at least 1,5 years of clinical research experience

As a member of an international Study Management Team under general supervision you will perform activities associated with study site initiation process according to applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. You will review and negotiate site regulatory documents and contracts with sites and sponsors for agreement on wording and budgets. You will review and provide feedback to management on site performance metrics.

At Quintiles we value individuality, fresh ideas, and the contribution that our employees make to our success. In return we offer career opportunities providing flexibility and growth across the organization, competitive salary and benefits package, work-life balance initiatives and social events. These are just some of the incentives we have to offer.

If you are interested in the position please visit our website www.quintiles.com/Careers and apply online via this website.

Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.