Location: Kyiv
Responsibilities: Assist CRAs and PMs in the course of daily work on clinical studies/receive experience and training to advance to CRA within 12 months.
1. Maintain Trial Master File and back-up files under direction of PM 2. Maintain meeting and teleconference minutes; assist with translations as needed 3. Maintain written and oral communication with sites and other study team members under direction of PM 4. Assist with CRA filing and scheduling as necessary 5. Other administrative tasks as requested by CRAs or PM
Qualification: University or other higher education. Any experience in clinical research (as investigator or CTA) would be preferred, but not necessary. Fluent English (written/spoken), strong communications ability, computer literate, organized, attentive to details.
Probation term: 3 months probation term at 100% salary When is first review of salary? 3 months (for probation period), then each 1 year What is the next step up for this person? Clinical Research Associate after 6-12 months of successful work as CTA and company training |