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FSP部門オンコロジー領域　CRA II～Sr CRAⅠ

年収：応相談

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部署・役職名	FSP部門オンコロジー領域　CRA II～Sr CRAⅠ
職種	CRA（臨床開発モニター）
業種	その他
勤務地	東京都
仕事内容	コロナ禍でも安定した収益を挙げているFSPチームの募集です。追加受注に伴い増員を行います。本プロジェクトはオンコロジー領域を担当していただく予定です。ご関心あればぜひ弊社採用チームまでお問合せください。ご応募をお待ちしております！ JOB SUMMARY The Clinical Research Associate II （CRA II） / the Senior Clinical Research Associate I （SCRA I）will perform monitoring and site management activities for Phase I－IV clinical research projects to assess the progress of clinical projects at assigned investigative/physician sites （either on site or remotely） and to ensure clinical projects are conducted, recorded, and reported in accordance with the protocol, Company and Sponsor standard operating procedures （SOPs）, ICH－GCP and/or all applicable local and federal regulatory requirements. Performs all tasks routinely and independently, seeking guidance as needed. May assume clinical functional leadership tasks as assigned, acting as Lead CRA for a project or assessor of peers for sign－off visit purposes （Sr. CRA）. JOB RESPONSIBILITIES ・Performs site qualification, site initiation, interim monitoring, site management activities and close－out visits （performed on－site or remotely） ensuring regulatory, ICH－GCP and/or Good Pharmacoepidemiology Practice （GPP） and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding sitespecific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. ・Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues. ・Per the Clinical Monitoring/Site Management Plan （CMP/SMP）: o Assesses site processes o Conducts Source Document Review of appropriate site source documents and medical records o Verifies required clinical data entered in the case report form （CRF） is accurate and complete via review of site source documents and medical records o Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines o Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture o Verifies site compliance with electronic data capture requirements ・May perform investigational product （IP） inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately （re）labelled, imported and released/returned. ・Routinely reviews the Investigator Site File （ISF） for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File （TMF）. Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations. ・Documents activities via confirmation letters, follow－up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution. ・For assigned activities, understands project scope, budgets, and timelines for own and others’ activities in the clinical team; manages site－level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets. （CRAⅡ）・Understands project scope, budgets, and timelines for own and others’ activities in the clinical team; manages site－level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets. （Sr. CRAⅠ）・May act as primary liaison with study site personnel / project site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project－specific site team members are trained and compliant with applicable　requirements. ・Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates, and may, with supervision, lead, in global clinical monitoring/project staff meetings （inclusive of Sponsor representation, as applicable） and attends clinical training sessions according to the project specific requirements. ・Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow－up actions. ・Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes; completes assigned training as required. （CRAⅡ）・May provide training or mentorship to more junior level CRAs. May perform training and sign off visits for junior CRA staff, as assigned. （Sr.CRAⅠ）・May be mentored and assigned clinical operations lead tasks under supervision of an experienced Clinical Operations Lead （COL）, or operational line manager. （Sr.CRAⅠ）・For Real World Late Phase, the CRA II will use the business card title of Site Management Associate （CRAⅡ）・For Real World Late Phase （RWLP）, the Sr. CRA I will use the business card title of Sr. Site Management Associate （Sr.CRAⅠ）・Additional responsibilities include: o Site support throughout the study lifecycle from site identification through close－out o Knowledge of local requirements for real world late phase study designs o Chart abstraction activities and data collection o Collaboration with Sponsor affiliates, medical science liaisonsand local country staff o The SMA II may be requested to train junior staff o Identify and communicate out of scope activities to Lead CRA/Project Manager o Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider （HCP） associations o Identify operational efficiencies and process improvements o Develop country level informed consent forms o Collaborate with RWLP Regulatory team to ensure updated regulatory information is applied and shared （Sr.CRAⅠ） o Participate in bid defense meetings （Sr.CRAⅠ）
応募資格	【必須（MUST）】 QUALIFICATION REQUIREMENTS ※オンコロジー領域2年以上の経験が必須です。・Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience ・Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements ・Must demonstrate good computer skills and be able to embrace new technologies ・Excellent communication, presentation and interpersonal skills. Basic level of critical thinking skills expected. ・Ability to manage required travel of up to 75％ on a regular basis
アピールポイント	自社サービス・製品あり外資系企業女性管理職実績あり上場企業従業員数1000人以上 2年連続売り上げ10％以上UP 年間休日120日以上産休・育休取得実績あり教育・研修制度充実資格支援制度充実社内公用語が英語シェアトップクラス完全土日休み
受動喫煙対策	その他「就業場所が屋外である」、「就業場所によって対策内容が異なる」、「対策内容は採用時までに通知する」などの場合がその他となります。面接時に詳しい内容をご確認ください
更新日	2024/08/16
求人番号	1912080

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