出海雷达

Experienced Clinical Research Associate (Remote, Guangzhou)

其他明确接受中国求职者
公司medpace
薪资未公开
工作地点China
地域资格明确接受中国求职者
时区要求日间重叠约 9 小时,基本正常作息
用工类型Full Time
发布时间今天
数据来源Himalayas
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明确接受中国求职者:该职位的地域要求包含中国,可正常投递。
关于本页中文:职位描述由本机离线模型翻译,属机器翻译,供快速判断用;正式沟通与投递请以英文原文为准。官方翻译通道恢复后会自动重译升级。

我们的临床活动正在迅速发展,我们目前正在寻找一个全职,本地临床研究员加入我们的临床运营团队在中国。如果你想有一个令人兴奋的职业生涯,在那里你可以使用你的以前的专业知识,并能够进一步发展和增长你的职业生涯。然后这是机会给你.Medpace 的临床研究人员提供独特的机会参与药物开发过程中的每一阶段,通过为客户提供无与伦比的支持。如果你想要一个令人兴奋的职业生涯,使用医疗或健康背景和教育,广泛旅行并在临床试验过程中发挥重要作用,这可能是你的机会。我们的成功临床研究合作伙伴拥有医学和相关卫生保健领域的多种背景。在 CRA 角色中取得成功的人包括注册护士,饮食师,药房技术人员,制药销售代表和研究助理。广泛的培训计划提供了有效和自信地履行你的工作平台。责任。· 开展可行性,预研究,启动,监测和关闭访问研究地点,主要是1至3阶段以及所有可用的治疗领域;· 进行源文件验证和案例报告表格审查;· 执行监管文件审查;· 研究药物库存;· 举报并跟踪不良事件和严重的不良事件;·评估患者招聘和保留。资格 · 在健康相关领域获得学士学位 (优先获得 BSN); · 最少有2年的经验证明的 CRA 经验;· 对医学术语和临床病人管理广泛知识;· 药物治疗技术和临床研究方法的基本知识;· 在当地语言和优秀英语中流利.Medpace Overview Medpace 是一个全服务临床合同研究组织 (CRO),为生物技术,制药和医疗设备行业提供 l-lV 阶段临床发展服务。我们的使命是通过临床研究的进步加速安全有效的医学疗法全球发展。我们利用国内监管和治疗专业知识在所有主要的治疗领域包括肿肿瘤学,心脏病学,代谢,内分泌学,中央神经系统以及抗病毒和抗感染等。总部位于辛西那提,.

查看英文原文

Our clinical activities are growing rapidly, and we are currently seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team in China. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivaled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacy Technicians, Pharmaceutical Sales Representatives and Research Assistants. An extensive training program provides the platform to effectively and confidently carry out your duties.

Responsibilities

  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 and within all available therapeutic areas;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.

Qualifications

  • Bachelor of Science in health-related field (a BSN is preferred);
  • Min. 2 years of proven CRA experience;
  • Broad knowledge of medical terminology and clinical patient management;
  • Basic knowledge of drug therapy techniques and clinical research methodologies;
  • Fluency in local language and excellent English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
· · Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
·
· Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
·
· Office based environment with on-site mentors

  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
·
· Competitive compensation programs that recognize and reward performance

  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Originally posted on Himalayas

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