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Clinical Research Associate (Freelance Role) at Biomapas. Freelance opportunity in Azerbaijan! . Interested to join our Clinical Operations team as a Clinical Research Associate (CRA) with regulatory and start up experience in Azerbaijan?.  . Clinical Research Associate . is responsible for monitoring clinical trials and ensuring compliance with regulatory requirements, study protocols, and standard operating procedures (SOPs)..  . This is a position for the potential activities in Azerbaijan, . working in close collaboration Clinical Operations team..  .  . You have energy and motivation to work in a team and to gain more experience? . Submit your CV in the English language for consideration..  . Responsibilities:.  . ·       Consulting of Clinical Operations team in country regulatory and start up requirements.. ·       Prepare clinical trial submission dossier and conduct CA and EC submission.. ·       Monitor clinical trials in accordance with regulatory and company guidelines.. ·       Conduct site initiation, monitoring, and close-out visits.. ·       Evaluate and ensure compliance with the study protocols, data integrity, and patient safety.. ·       Maintain communication with clinical trial sites and address any issues that arise.. ·       Collect, review, and verify clinical data for accuracy and completeness.. ·       Assist in the preparation of study documentation and reports.. ·       Keep updated with industry guidelines and regulatory changes. . ·       University degree in Life Sciences, Nursing, or related field. . ·       Fluent written and spoken English and native Azerbaijani.. ·       At least 1-2 years of experience as a Clinical Research Associate or in a similar role.. ·       Strong understanding of Good Clinical Practice (GCP) and regulatory requirements. . ·       Excellent organizational and time management skills.. ·       Ability to work independently and as a part of a team.. ·       Proficient in using electronic data capture systems and MS Office.. Company Location: Azerbaijan.