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Senior Site Management Associate

Published on 19.09.2023


ICON Strategic Solutions is the global leading provider of Functional Service Provision (FSP) services. Through combined functional, operational,... read more

Job Ad & Profile Description

Position : Senior Site Management Associate

As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


You will be joining one of our global pharmaceutical clients, working within an organisation that is focused on improving lives of people with cancer through innovative targeted therapies.


What you will be doing:

  • Create and maintain clinical trial documents.
  • Participate in the identification, evaluation, and selection of clinical trial sites.
  • Conduct data review.
  • Responsible for tracking of ancillary and investigational supplies, specimens and/or imaging.
  • Support CTMS and Trial Master File completeness.
  • Support audit and/or inspection activities
  • May manage CRO activities.
  • Support Clinical Trial Manager(s). Collaborates with internal team members, Contract Research Organizations, vendors and sites.
  • Work on problems of diverse scope where analysis of data requires evaluation of identifiable factors.
  • Perform all duties and responsibilities in accordance with CFR, GCP/ICH Guidelines, SOPs, and other applicable guidelines.
  • May contribute to process improvement initiatives and departmental projects.
  • May act as mentor for less senior staff on the study.


    Required profile for job ad : Senior Site Management Associate

    You are:

    • BA/BS or equivalent or any relevant and qualifying training with a minimum of 2+ years of relevant clinical trial management experience.
    • Oncology clinical research experience
    • Regional Clinical Trial Management experience
    • Excellent leadership, communication, and organizational skills. Able to multi-task under limited direction and on own initiative.
    • Ability to proactively handle multiple tasks, manage a diverse range of functional activities and solve problems simultaneously.
    • Strong communication and inter-personal skills.
    • Highly responsive and proactive, a team player
    • Knowledge of CFR and GCP/ICH requirements
    • Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF)
    • Ability and willingness to travel
    • Fluency in English
    Job criteria for job ad : Senior Site Management Associate
    Job category :
    Industries :
    Pharmaceutical industry
    Employment type :
    Permanent contract - Fixed-term contract
    Region :
    Arusha - Dar es Salaam - Dodoma - Geita - Iringa - Kagera - Katavi - Kigoma - Kilimanjaro - Lindi - Manyara - Mara - Mbeya - Morogoro - Mtwara - Mwanza - Njombe - Pemba - Pwani - Rukwa - Ruvuma - Shinyanga - Simiyu - Singida - Songwe - Tabora - Tanga - Zanzibar - International
    Experience level :
    2 to 5 years
    Educational level :
    Spoken language :
    Key Skills :
    Number of Position(s) : 1
    Be cautious! Do not send money to a potential employer. Do not pay any money for a potential contract of employment or for pre-employment training.
    Please report any irregularities by using the candidate contact form and selecting the subject "Report a job ad".

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