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: Sep 21, 2021
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Bioforum is a data focused CRO, offering a wide range of consulting services, medical writing, data management and bio-statistical support. We are a multi disciplinary team of experts that helps clients comprehend the value of their clinical data simply by making it readily available for monitoring, analysis and ready for submission. Adhering To The High...
    Read more about this company

     

    Clinical Data Manager

    About Jobs

    Bioforum, bursting with opportunity!

    Data Managers based in South Africa Bloemfontein, what’s the next step in your career? 

    Minimum requirements:

    • Bachelor’s degree or above in a biomedical or science discipline and equivalent experience is required.

    Minimum experience:

    • Working in a data management role for at least 2 years

    Minimum requirement/skills:

    - Knowledge of clinical trial process flow.

    - Microsoft Office and EDCs knowledge is required.

    Minimum requirement/competencies:

    - English proficiency is required.

    Responsibilities:

    •  Collaborate with Project Managers in study documents and deliveries
    •  Ensure clinical trial data integrity and consistency
    •  Review study specific protocols and assist in the design of CRF utilizing company and/or sponsor data standards as applicable, collaborating with Project Managers and Head of Data Operations  Hands on study data review including clinical database and external data according to Project Manager guidance
    •  Collaborate in defining study specific Data Checks (automated and manual)
    •  Collaborate in Data Management Plan creation
    •  Perform data validation efforts prior to go live and as applicable during study
    •  Depending on qualifications, perform manual coding as needed according to Coding Plan and Coder guidance
    •  Responsible for planning data review for completeness prior to milestones and notifying Project Managers regarding workload and ensuring resources are adequate to meet the timelines
    •  Ensure all study documents are saved under the relevant study files
    •  Supervise and mentor other Data management and/or Clinical Quality Control associates
    •  Contribute to departmental SOP development
    •  Training new employees

    Typical tasks:

    • Typical data management activities as well as providing input and support to process improvements and training.

    Method of Application

    Interested and qualified? Go to Bioforum the Data Masters on bioforum.bamboohr.com to apply

    Note: Never pay for any training, certificate, assessment, or testing to the recruiter.

  • Send your application

    View All Vacancies at Bioforum the Data Masters Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
 
Send your application through

GmailGmail YahoomailYahoomail