CLINICAL RESEARCH ASSOCIATE (freelancers or project based interested professionals)

Completes project activities associated with monitoring functions Phase I-IV clinical research studies while developing an understanting of the drug development process, Good Clinical Practices, and relevant regulations.

Performs management of study site activities to ensure the integrity of clinical data,in adherence to all applicable regulatory guidelines and Standard Operating Procedures (SOPs) and Project Specific Operating Procedures (PSOPs).





 

- Previous experience of minimum 3-5 years;

- University degree in Medicine, Pharmacy, would be a plus;

- A clean driving license;

- Very good proficiency in English;

- Excellent interpersonal, organizational skills and the ability to adapt to international environment;

- An enthusiastic personality and a self-motivated individual;

A dynamic career in a multinational company Excellent salary package depending on experience and qualifications. The possibility to work in a professional environment.