廣州天河區(qū)珠江新城

項(xiàng)目及治療領(lǐng)域：
負(fù)責(zé)global II/III期腫瘤項(xiàng)目

公司提供豐厚的薪資福利: 五險一金，補(bǔ)充公積金，生日/節(jié)假日禮品券，spotlight積分兌換商品
額外津貼：住房補(bǔ)充，交通，餐飲，采暖（僅適用于中國北方地區(qū)）等各種津貼
員工健康：補(bǔ)充商業(yè)醫(yī)療保險，年度健康體檢
長期發(fā)展：內(nèi)部轉(zhuǎn)崗機(jī)會，豐富的線上線下培訓(xùn)
專業(yè)培訓(xùn)：Clinical Training Institute的專業(yè)支持，賽紐仕的CRA培訓(xùn)計(jì)劃由IAOCR認(rèn)證并頒發(fā)相應(yīng)證書

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 site-specific 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
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; 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.
? May act as primary liaison with study 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 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.
? For Real World Late Phase, the CRA II will use the business card title of Site Management Associate II. 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 liaisons and 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
Qualifications
What we’re looking for
? Bachelor’s degree and or above degree with major in medicine/healthcare/life science related
? 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
? Ability to manage required travel of up to 75% on a regular basis
Syneos Health賽紐仕醫(yī)藥是一家全面整合生物制藥解決方案的公司，旨在幫助客戶加快推出新療法的速度。我們站在產(chǎn)品研發(fā)的角度，戰(zhàn)略性地融合臨床研發(fā)、醫(yī)學(xué)事務(wù)和商業(yè)能力，以及時應(yīng)對最新市場變化。 想了解更多關(guān)于我們?nèi)绾慰s短從實(shí)驗(yàn)室到現(xiàn)實(shí)生活的距離，請?jiān)L問官網(wǎng)或訂閱我們的播客。