TPM requires an experienced freelance home-based Clinical Research Associate to work on a global, long-term cardiovascular phase III clinical trial in Latvia.
Your responsibilities will include clinical monitoring activities through to close-out as well as active participation in local investigator meetings and on-going training throughout the trial.
The ideal candidate will be a self-sufficient clinical research professional who recognises the value of a long-term collaboration with a major player in the pharmaceutical industry.
A medical or life science degree or nursing equivalent with fluency in Latvian and English is a must. Fluency in Russian is an advantage. You will need strong interpersonal and communication skills as well as being computer literate. Candidates should be flexible, willing to travel within Latvia and abroad and have a valid driver’s licence. Experience as a CRA with a minimum of 2 years previous monitoring experience is required.
Successful candidates will be employed on a freelance basis and will receive a competitive hourly rate and generous travel and subsistence allowances as well as reimbursement of all office expenses and telephone costs.
Extensive training and company laptop will be provided and there will be regular opportunities to travel outside of Latvia.
Please send your application letter with CV in English by the 15th July 2011 to: Pille Mägi, email: firstname.lastname@example.org