Medical Information Specialist-Clinical Trials with Czech & English
Core
Provide technical, medical, and clinical trial information to support the recruitment, engagement, and pre-screening of potential clinical trial participants via virtual interactions.
Role type
Medical Information Specialist (Clinical Trials)
Builds
Patient recruitment pipelines and clinical trial participant engagement
Domain
Clinical Research / Pharmaceutical Trials
Deliverable
client delivery
Required skills
Czech (fluent), English (fluent), medical literature research, adverse event triage, protocol-specific pre-screening, regulatory guideline adherence
Preferred skills
Medical, Pharmacy, or Biomedical degree background
Technologies
Study-specific questionnaires, checklists, designated clinical databases
Responsibilities
Conduct inbound and outbound patient recruitment activities; respond to technical and medical inquiries via phone, email, or internet; analyze caller questions and formulate accurate responses using approved resources; complete and document study-specific questionnaires and pre-screening results; coordinate scheduling and referral of eligible participants to clinical research sites; identify, record, and triage adverse events and product complaints; maintain knowledge of GCPs, protocols, and regulatory requirements.
Seniority
Entry-level to Junior (0-2 years experience)
