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Job Overview
CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the relationship management and communication of medical and scientific information with health-care providers, patients, care givers.

Essential Functions
• Works with research sites to develop study-specific action plans to accelerate patient recruitment or support study-specific procedure training
• Provides education to health care professionals and their staff,  reinforces study protocols as related to a clinical trial
• May have direct interaction with patients to offer education on trial, disease, and/or device/medication. Partner with referral networks to itentify potential trial subjects.
• May partner with referral networks to identify potential subjects for a trial;
• maintains and analyzes customer records to customize strategies to maximize patient pre-screening, screening, enrollment in trial
• completes internal electronic reporting systems; organizes and holds group events to optimize program delivery; successfully manages objections raised;
• maintains organization equipment safely and in a good state of repair
• and maintains up-to-date technical knowledge of specialty and disease areas.

Qualifications

• Cardiovascular/Oncology/CNS trials 경험이 있는 Study Coordinator 지원 가능
• Bachelor's Degree BS in Health Sciences or related field or equivalent academic professional qualifications.
• Typically requires 1 - 2 years of prior relevant experience (CRA exp. preferred)
• Clinical competence in relevant therapeutic area : SIV, Recruitment period, Cardiovascular study exp. preferred
• Excellent interpersonal and English communication skills
• Strong customer service approach
• High flexibility to travel, team player for the good of the tea