崗位職責(zé):
主要職能:
Key Objectives/Deliverables:
1.根據(jù)試驗(yàn)方案、SOP、GCP和相關(guān)的當(dāng)?shù)胤ㄒ?guī)的要求進(jìn)行研究中心篩選、啟動、監(jiān)查和關(guān)閉訪視。
2.可同時負(fù)責(zé)多個方案、研究中心和治療領(lǐng)域內(nèi)的研究中心監(jiān)查工作。
3.根據(jù)每個研究中心的情況制定項目受試者的招募計劃。根據(jù)項目需要與研究中心合作,調(diào)整、推動和跟蹤受試者招聘計劃,以提高招募進(jìn)度的可預(yù)見性。
4.對所負(fù)責(zé)的研究中心進(jìn)行方案和研究相關(guān)的培訓(xùn),與研究中心進(jìn)行定期溝通以管理項目進(jìn)行中的要求和問題。
5.評估研究中心工作的質(zhì)量和完整性,確定研究中心是否是按照方案和適用的法規(guī)進(jìn)行研究,確定受試者的權(quán)益受到保護(hù)。將質(zhì)量問題匯報給負(fù)責(zé)的PM和/或直線經(jīng)理。
6.通過追蹤注冊申報和批復(fù)、招募和入選、病例報告表(CRF)完成和遞交、以及數(shù)據(jù)疑問產(chǎn)生和解決的情況,管理所負(fù)責(zé)研究中心的進(jìn)展。
7.創(chuàng)建和維護(hù)與研究中心管理、監(jiān)查訪視的發(fā)現(xiàn)以及行動計劃相關(guān)的文件,遞交訪視報告和其他所需研究文件。
8.負(fù)責(zé)相應(yīng)研究中心的研究財務(wù)管理。
9.與其他職能部門共同合作。
10.對于公司外包項目,協(xié)助協(xié)調(diào)CRO、研究中心和服務(wù)商,建立并保持良好的關(guān)系。
11.完成直線經(jīng)理和/或項目經(jīng)理分配的其他工作。
Key Responsibilities:
1.Perform site selection, site initiation, monitoring and close out visits in accordance with protocol, SOPs, GCP and applicable local regulations.
2.Responsible for sites monitoring related works in multiple protocols, sites and therapeutics areas.
3.Accountable for supporting development of project subject recruitment plan on a per site status. Work with site to adapt, drive and track subject recruitment plan in the line with project needs to enhance predictability.
4.Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
5.Evaluated the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
6.Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission and data query generation and solution.
7.Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow up letters and other required study documentations.
8.Responsible for site study financial management.
9.Collaborate and liaise with study team members for project execution support as appropriate.
10.Assistant for cooperating with CRO, site and vender to build up good relationship.
11.Complete other tasks assigned by line manager and project manager.
任職要求:
1.良好的臨床研究相關(guān)知識,了解適用的法規(guī)要求,至少一年以上腫瘤項目經(jīng)驗(yàn)。
2.通過公司培訓(xùn)掌握方案相關(guān)的知識。
3.良好的計算機(jī)使用技能,包括應(yīng)用微軟Word、Excel和PowerPoint等。
4.良好的口頭和書面溝通能力。
5.良好的組織和解決問題的能力。
6.與同事、經(jīng)理、研究中心和服務(wù)商建立工作關(guān)系的能力。
7.能始終遵循SOP要求。
Qualifications:
1.Good knowledge of clinical research and understanding of applicable regulatory requirements,at least 1 year of oncology experience.
2.Master the protocol related knowledge required through company training.
3.Good computer skills, including proficiency in Microsoft Word, Excel and PowerPoint
4.Good verbal and written communication skills.
5.Good organization and problem solving skills.
6.Effective time management skills, ability to handle conflicting tasks at the same time.
7.Ability to establish and maintain effective working relationships with colleagues, managers, research centers, and service providers.
8.Can always follow SOP requirements. Ability to think independently and improve process.