Company offers:

- Excellent rates (depending on experience)
- A new challenge and prospects of career progression within a growing company
- A high level of responsibility and independence
- A supportive and friendly working environment


Requirements:

- Life science degree (medical, paramedical, pharmacy, biochemistry field is preferred)
- At least 2.5 years experience as a Clinical Research Associate / Monitor in a Contract Research Organization (CRO) or Pharmaceutical company
- Good organizational skills with ability to work diligent, accurate and under pressure, alone or as part of a team
- Computer literacy (Microsoft Office Tools)
- Curiosity and willingness to improve skill set (self training)
- Good communication skills
- Prepared to travel locally and internationally (at least 50% of working time)
- Fluency in Latvian and English, both written and spoken (Russian is a definate advantage)


Main Duties & Responsibilities:

- Reporting directly to the CTL or MD
- Site selection and feasibilities
- Regulatory and ethics submissions
- Monitoring visits
- Study tracking and close-outs


If you are interested in this position or know someone who might be suitable/interested, please feel free to contact me or pass my contact details for further information.


SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business