We invite for cooperation both on full-time and free-lance basis CRAs, full-time Project Managers, and Project Assistants in the following countries:
· Russia
· Ukraine
· Bulgaria
· Latvia
· Lithuania
· Estonia
· Hungary
If interested in cooperation, please send your CV to job@out-clinicaltrials.com
Immediate Openings
» Clinical Research Associate (CRA)
We are looking for a highly qualified candidate for position of a full-time and part-time clinical trial monitors.
Requirements: Medical degree (MD) or PHD in life science is required. Experience as a CRA or Principal Investigator, Sub-Investigator, Study Coordinator for at least one year is a must. The candidate should be highly motivated, responsible, willing to travel on as needed basis (up to 50% travel is anticipated) and have advanced level of written and spoken English.
Please submit your CV and cover letter to job@out-clinicaltrials.com
» Home-based Clinical Research Associate (CRA)
We are looking for qualified candidates for position of a home-based clinical trial monitors. This position presumes primarily responsibilities of monitoring (pre-study, initiation, monitoring, and close-out visits) of investigator sites for the compliance to the protocol, ICH GCP, client SOPs and applicable local regulations. Up to 50% travel is anticipated. The responsibilities may also include recruiting investigators for participation in the clinical trials, negotiate investigator clinic contracts, obtain, review for appropriateness, and process regulatory and administrative documents from the investigator sites.
Requirements: Medical degree (MD) or degree in life science is required. Experience as a CRA, Principal Investigator, Sub-investigator or Study Coordinator is a plus. The candidate should be highly motivated, responsible, willing to travel on an as needed basis and have good command of written and spoken English.
Please submit your CV and cover letter to job@out-clinicaltrials.com
» Project Manager (PM)
PM manages the work of CRAs and Clinical Trials Coordinators/Assistants and coordinates project-specific activity of other company’s departments and outside vendors to ensure that clinical trials are conducted in accordance with GCP, local regulatory requirements and highest quality standards within the timelines and budget stipulated by the contract. Main activities include: project planning, project team building, project team managing, organization and conducting of study related meetings and trainings, coordination of study logistics, creation of study specific documentation, checking of all types of CRA reports, reporting to and communication with sponsors, administration of investigator’s and hospital payments, coordination of activity of all company’s departments involved in the project, others.
Requirements: Medical Doctor, fluent English (written and spoken), Project Manager or Senior CRA experience, sound management skills, well-developed communication skills, results oriented.
Please submit your CV and cover letter to job@out-clinicaltrials.com
» Clinical Trial Coordinator/Assistant
Clinical Trial Coordinator (CTC) coordinates the work of CRAs and gives assist to Project Manager to conduct clinical trials. Main activities include: assistance in organization and holding of study related meetings/trainings, reporting and communication with sponsor, assistance in preparation and reporting of project status, controlling investigators’ invoices, assistance in coordination of activity of all departments and units involved in the project, assistance in creation of study specific procedures, preparation of investigator files, maintenance of TMF, study documents translation, application of FDA forms, assistance in regulatory package preparation and submission, assistance in preparation of financial reports, others.
Requirements: High education, excellent English and Russian (spoken and written), ability to work under demanding time schedules, strong leadership and ability to learn, presentation skills.
Please submit your CV and cover letter to job@out-clinicaltrials.com
