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Experienced Clinical Research Associate (Remote, Guangzhou)

Role overview

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

Responsibilities

  • Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites, mainly phase 1 to 3 within all available therapeutic areas
  • Perform source document verification and case report form review
  • Perform regulatory document review
  • Conduct study drug inventory

Key facts

Other skills

  • Communication
  • Collaboration
  • Decision Making

About the company

Medpace logo

Medpace

Contract Research Organizations (CRO)

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 5,800 people across 43 countries.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size5001 - 10000

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Job description

Job Summary :

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.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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