Pfizer Hiring Clinical Data Manager – Clinical Data Sciences

Pfizer Hiring Clinical Data Manager – Clinical Data Sciences

4 April, 2022

JD –

  • Manage own time to meet agreed targets; develop plans for work activities on own projects within a team.
  • Serve as Data Manager for one or more clinical trials assuming responsibility for Data Monitoring and Management (DMM) activities.
  • Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan.
  • Ensure operational excellence across all Data Monitoring and Management (DMM) deliverables.
  • Set-up and test data review listings to verify the quality and completeness of data as specified in Data Management Plan by reviewing data attributes populated by general users.
  • Ensure lessons learnt during the study are documented and shared with other study teams to facilitate cross-study learning.
  • Build good relationships with local and global SMEs from different fields, leverage their expertise in areas such as systems and process and proactively identify issues and work to create solutions.



  • Bachelor’s Degree
  • 3+ years’ experience
  • Demonstrated knowledge of data management processes and principles
  • Experience with web based data management systems
  • Working knowledge of electronic document management systems
  • Knowledge of International Conference on Harmonization and more specifically Good Clinical Practices
  • Thorough understanding of the processes associated with clinical study management and regulatory operations
  • Ability to manage tasks, time and priorities
  • Demonstrated effective verbal and written communication skills and adapt communications to audience


  • Master’s degree
  • Relevant pharmaceutical industry experience
  • Experience using data visualization tools
  • Proficient experience using commercial clinical data management systems and/or EDC products
  • Awareness of regulatory requirements and relevant data standards

Apply through this link


  • Dear Sir/Madam,

    I am Shubham Rangoli, an M Pharm graduate and Currently working as Senior Officer in QA Dept at Intas pharmaceuticals Limited, Ahmedabad. (Since Sept-2021).

    Completed “Pharmacovigilance Training Programme” Conducted by Pharma Times

    Depth knowledge in Reviewing BMR/ BPR.

    I am very much Interested to work within your Organization.

    Ready to Join Immediately.

    Please find my attached Resume For more details.

    I look forward to hearing from you.

    Shubham Rangoli

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