Clinical Research Advisor

Cobel Darou Tehran

Posted 3 months ago

Job Description

• Accountable for all aspects and progress of clinical trial from study planning activities to study execution. • Verify that the researcher has adequate qualifications and resources, as well as facilities, including laboratories, equipment and staff are adequate for safety and properly conduct of the clinical study throughout the study period. • Identify and resolve the issues (logistical, methodological, and technical) proactively occurring during a study and recommend solutions. • Proper collection and archiving the essential study documentation. • Timely and accurately execution of monitoring plan. • Prepare reports based on demand; prepare adverse event report and progression report. • Ensures realization of expenses and planned budget are balanced and tracks accordingly.

Requirements

• Educational background MD, Pharmacist, PhD, DVM. • Sound knowledge of medical terminology and clinical monitoring process. • Being familiar to clinical research operations, and implementing MOH regulations and guidelines. • Excellent interpersonal savvy. • Strong attention to detail and excellent organizational skills. • Strong focus on continuous learning. • Proficiency in Office suite, including Word, Excel, PowerPoint skills. • Fluent in English. • Flexibility to travel.

Job Category:

Healthcare - Pharmaceutical

Healthcare - Physician & MD

Employement type:

Full Time

Job Category:

Healthcare - Pharmaceutical

Healthcare - Physician & MD

Employement type:

Full Time

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