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: Nov 25, 2020
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Want to get a job fast? Signup and complete your profile on MyJobMag. Employers will find you 4x faster with a complete profile. You can download your completed profile anytime
    With 46 years’ experience in successful job-matching and placement of top candidates, Kelly - a division of Kelly Group - forms a part of Adcorp Holdings Limited (listed on the JSE in 1987), ), South Africa’s leading provider of staffing, human capital management and business process outsourcing services, we have access to financial resources, le...
    Read more about this company

     

    Clinical Trial Project Leader (Pharmaceuticals)

    Introduction

    We're seeking a Clinical Trial Project Leader (Pharmaceuticals) – Midrand to be responsible for allocated clinical trials/studies within the cluster, ensuring compliance with the companies quality standards and processes, regulations in force, the forecasted

    Duties & Responsibilities

    •  Overall responsible and accountable for allocated clinical trials within the Clinical Study Unit.
    •  All study related activities at various stages of a clinical study – start up, recruitment, maintenance,close out and archiving.
    • Study activities performed according to Good Clinical Practice, regulations in force and company standards and processes.
    • Supports the management team in driving the Clinical Study Unit       
    • Primary contact with identified key stakeholders - Ensures appropriate communication and support with these stakeholders.
    • Selection of clinical trial sites.
    • Submissions to Ethics Committees / IRBs
    • Training of sponsor and clinical trial personnel on study related processes and requirements.
    • Contract negotiation and agreement with Clinical Trial sites.
    • Maintaining clinical study documentation in an audit ready state.
    • Compliance with requirements to all study related databases.
    • High quality standards of study data collection and prompt data query resolution.
    • Adequate provisioning of study materials and devices.
    • Oversee monitoring activities through regular contacts with local monitoring team, local teammeetings, review of monitoring visit reports and adherence to the monitoing plan.
    • Preparation and prompt responses to audit/inspection reports and implementation of recommendations.

    Desired Experience & Qualification

    • University degree in Health Sciences or equivalent
    • Clinical Research experience essential, minimum 5 years
    • Knowledge of GCP/ICH phase I-IV clinical trials
    • Computer skills must include working knowledge of Excel, PowerPoint,
    • Word and Outlook
    • Project and people management skills
    • Organizational, analytical and planning abilities
    • Fluent in English
    • Literate in French will be an advantage

    Package & Remuneration

    • Permanent
    • Market Related 

    Method of Application

    Interested?

    • Email your CV to Jobs@Kelly.co.za .
    • N.B. If you're emailing us directly, remember to insert : "Clinical Trial Project Leader (Pharmaceuticals) – Midrand" in the email subject line, for consideration

    Learn how to get a job in any industry you want. Read 72 Hours to The Job You Love

  • Send your application

Back To Home

Career Advice

View All Career Advice

Subscribe to Job Alert

 

Join our happy subscribers

This website uses cookies to improve your experience. By using this site you agree to the storing of cookies on your device to enhance navigation, analyze site usage, and assist in our marketing efforts. To learn more, see our Cookie Policy. Accept and Close
 
 
 
Send your application through

Yahoomail Gmail Hotmail