临床协调员crc

岗位职责 / Job Responsibilities 1. 数据与信息管理 / Data and Information Management 负责受试者数据库的建立与日常管理，确保信息录入的准确性与及时性； Establish and manage the subject database on a daily basis, ensuring the accuracy and timeliness of data entry. 2. 受试者随访管理 / Subject Follow-up Management 负责受试者日常随访的预约、提醒及行程安排，保障访视按计划顺利进行； Handle the scheduling, reminders, and arrangements for subjects' routine follow-up visits, ensuring visits proceed smoothly as planned. 3. 研究者文件夹（ISF）管理 / Investigator Site File (ISF) Management 负责研究者文件夹的建立、日常维护与更新，确保试验文档的完整性与合规性； Establish, maintain, and update the Investigator Site File (ISF) on a daily basis, ensuring the completeness and compliance of trial documents. 4. 物资与药品管理 / Supplies and IP Management 负责研究文件、试验药品及相关物品的接收、发放、保存、清点和归还，并做好相关记录与台账管理； Manage the receiving, dispensing, storage, inventory, and return of study documents, Investigational Products (IP), and related supplies, maintaining accurate records and logs. 5. 数据录入与核对 / Data Entry and Verification 协助研究者完成病例报告表（CRF）的数据录入，并进行源数据核对，确保数据的真实、准确与可溯源； Assist investigators with the data entry of Case Report Forms (CRF) and conduct source data verification (SDV) to ensure data authenticity, accuracy, and traceability. 6. 多方沟通协调 / Multi-party Communication and Coordination 作为沟通桥梁，高效协调临床监查员（CRA）与研究者之间的沟通，协助准备监查访视文档，推进项目顺利开展。 Act as a communication bridge to effectively coordinate between Clinical Research Associates (CRAs) and investigators, assist in preparing for monitoring visit documents, and facilitate the smooth progress of the project. 任职要求 / Qualifications 1. 学历与专业 / Education & Major 本科及以上学历，临床医学、药学、护理学、生物等相关专业优先；（有丰富CRC项目经验者可放宽） Bachelor’s degree or above, majoring in Clinical Medicine, Pharmacy, Nursing, Biology, or related fields preferred. (Relaxation of educational requirements for candidates with extensive CRC project experience.) 2. 工作经验 / Work Experience 有1~3年 CRC或临床试验相关工作经验者优先； 1-3 years of working experience as a CRC or in clinical trials is preferred. 3. 核心能力 / Core Competencies 熟悉GCP法规及临床试验基本流程； Familiarity with GCP regulations and basic clinical trial processes. 具备优秀的沟通协调能力、抗压能力及团队合作精神； Excellent communication and coordination skills, strong ability to work under pressure, and a strong team spirit. 工作细致严谨，责任心强，对数据敏感； Meticulous and rigorous work style, strong sense of responsibility, and high sensitivity to data. 4. 其他要求 / Other Requirements 熟练使用Word、Excel等办公软件，具备良好的英语读写能力（CET-4） Benefits & Employee Care 基础保障 / Basic Protection 入职即缴纳五险一金。享受中外法定节假日、带薪年假、公司福利假； Social insurance and housing fund (Five Insurances and One Fund) will be paid upon employment. Enjoy statutory holidays (both Chinese and international), paid annual leave, and company welfare leave. 成长体系 / Growth System 提供系统化的GCP培训、一对一导师带教、清晰的晋升通道（初级CRC → 高级CRC → 项目经理）； We provide a systematic GCP training program and one-on-one mentorship, along with a clear career progression path (Junior CRC → Senior CRC → Project Manager). 员工关怀 / Employee Care 年度体检、节日福利、定期团建、交通/通讯补贴等。 Annual physical examination, holiday benefits, regular team-building activities, and transportation/communication allowances, etc.