■職務概要
クリニカルトライアルエデュケーター（CTE）は、担当試験の治験実施施設の患者登録において障害となっていることを特定・分析し、患者登録促進のための提案をします。

■職務詳細
・治験実施医療機関訪問（オンサイトあるいはリモート面会）、電話・メールによるコンタクト
・治験で使用する機器の使用方法についてトレーニングの実施（看護師に限る）
・各種レポート作成、クライアント会議への出席と報告、社内会議への出席と情報共有 など

■応募要件

▼以下条件をすべて満たす方
　・大学卒以上 （看護師の方は3年制の短大・専門学校卒業も可）
　・施設訪問（外勤）、宿泊出張ができる方
▼上記に加え、以下のいずれかのご経験をお持ちの方
・看護師としての勤務経験が7年以上あり、大学病院やがんセンター等での勤務経験、循環器内科、呼吸器内科、救急科、精神科、消化器内科などの勤務経験がある方
・看護師としての勤務経験が2年以上あり、治験コーディネーター（CRC）または臨床開発モニター（CRA）の経験が2年以上ある方
・薬剤師または臨床検査技師としての勤務経験が2年以上あり、治験コーディネーター（CRC）または臨床開発モニター（CRA）の経験が5年程度ある方
・治験コーディネーター（CRC）または臨床開発モニター（CRA）の経験が7年以上ある方

▼以下スキルがあるとなお望ましいです
　・英語でコミュニケーションがとれる方

Job Overview
As our specialist CTE, you will be able to accelerate patient enrollment, improve site performance and help streamline studies in ways no other team member can. You’ll often be your sites’ go-to person for information, advice and problem solving. You will also have the chance to work on studies featuring complex or non-traditional patient pathways often featuring compressed timelines for diagnosis and enrollment and complex protocols requiring intense initial education and ongoing reinforcement. It will be your role to help to navigate issues where intense competition exists for similar patient populations. You will also be needed to provide regular training and assistance for site staff and patients on issues such as drug administration and testing.

Essential Functions
• Provide practical support to study sites to maximize potential for patient enrolment.
• Work with research sites to identify and address recruitment barriers – identify common site issues and work with the sponsor and relevant stakeholders to recommend creative options to overcome these barriers.
• Provide on-going training and information on the clinical trial inclusion and exclusion criteria to the study team, where required conduct training for new study staff.
• Act as a resource for healthcare professionals at clinical study sites by sharing best practices and strategies for patient identification and retention.
• Conduct recruitment training sessions
• Identify patient flow / pathway through site and work with identified departments to raise awareness of protocols and the potential for patient inclusion.

Qualifications
• Bachelor's Degree Bachelor's Degree Req
• Experience working in a Clinical Trial Environment.
• Ability to coordinate activities across multiple functions and drive them to completion.
• Have a solutions based approach to addressing the identified barriers to recruitment.
• Good Business and Commercial acumen.
• English and Japanese language is essential.
• Ability to make rapid and accurate assessments.
• Excellent interpersonal and communication skills.
• Highly motivated well organised and results oriented.
• Flexibility to travel both nationally and internationally.
• Driving Licence required.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com