Jobs Career Advice Signup
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Apr 15, 2021
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Never pay for any CBT, test or assessment as part of any recruitment process. When in doubt, contact us

    PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and more than 19,000 professionals worldwide, PPD applie...
    Read more about this company

     

    Clinical Trial Coordinator

    We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients.  

    Additional Key Responsibilities Include

    Our clinical department defines, develops and delivers clinical programmes, ensuring the highest-quality review of data and effective interaction with study sites. As a Clinical Trial Coordinator, you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.

    • Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
    • Reviews regulatory documents for proper content
    • Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
    • Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
    • Assists with the identification of potential investigators and development/distribution of initial protocol packets
    • Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes

    Job Qualification
    Qualifications
    Education and Experience:

    • University degree, or equivalent in education, training and experience
    • Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout
    • Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
    • Experience of manage multiple projects with differing priorities at one given time
    • Exceptional communication, collaboration, organisational and time management skills

    Method of Application

    Interested and qualified? Go to PPD on careers.ppdi.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at PPD Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
Send your application through

GmailGmail YahoomailYahoomail