Location: Russia (Saint Petersburg, Moscow); Ukraine; Latvia; Lithuania; Estonia; Georgia; Bulgaria.
Company Name : Accell Clinical Research
Job summary: The Clinical Research Associate monitors activities at clinical study sites to assure adherence to Good Clinical Practice (GCP), SOPs, and study protocols. CRA assists Investigators to solve all study related issues, including communication with the study sponsor concerning clinical questions raised from the investigators. CRA reviews regulatory documents as required and prepares site visit reports. CRA may be involved in translations into the local language, developing study documents for local use, interaction with local regulatory and ethic authorities, performing translation and country-specific adaptation of Informed Consent (IC) forms, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training.
CRA will participate in clinical training programs and maintain awareness of developments in the field of clinical research.
Qualifications:
- Prefer University degree in medicine, pharmacy or life sciences
- Customer service orientation
- At least 1 year experience in clinical trials activities (Pharmaceutical Company, CRO or Investigational site)
- Fluent English, written and spoken
- Ability to work both independently and as part of the team, and time management skills
- Well-developed interpersonal and communication skills and attention to detail
- Ability to effectively coordinate all aspects of clinical trials across all relevant departments and involved sites/vendors
- Computer literacy, proficiency in MS Office
- Ability to travel approximately 30-50 % of working time
Please submit your CV to job@accellclinical.com
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