Job Description
Developing and writing trial protocols
Archiving study documentation and correspondence
Designing data collection forms
Monitoring the trial throughout its duration
Filing and collating trial documentation and reports
Assist with preparation of required regulatory submissions.
Assist with the design of CRFs as agreed within the project team.
Review all data produced from each study and resolve any data queries/protocol deviations identified.
Ensure that data is provided to the Data Manager in a timely manner for databasing.

Required Skills and Knowledge
University Degree in Life Science Sector (Biology, Chemistry, Pharmacy, Nursing)
Post-graduate degree will be considered as an additional asset
1-2 years of relevant experience
Excellent command of Greek and English language
Excellent Computer Skills
Ability to travel frequently (both locally and abroad)
Self-motivated and able to work independently in a highly demanding multinational environment
Goal - oriented personality
Excellent communication and negotiation skills
Strong presentation skills
Effective time management skills
Team player
Valid Driving licence/Passport

The company offers:
Highly competitive remuneration package plus performance bonus
Company car and mobile phone
Private medical insurance
Excellent working environment
Continuous training and fast track career development opportunities
Opportunities for an International career

Please send your full cv through e-mail
fax: 210 3259380