Apply for the position of Clinical Data Analyst at Sitero – B. Pharma/ M. Pharma/ Lifescience

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Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. 

Name of Post: Clinical Data Analyst

Function: Clinical Operations

Job Description: Clinical Data Analyst is a safety professional responsible for assessing and entering all the subject related information into Electronic Data Capture Systems in clinical trials. Using standard guidelines, they capture, review and enter all subject related data into given EDC systems.

Essential Roles and Responsibilities:

  • Analyzes, reviews, and interprets subject data from clinical trials and enters them into EDC systems
  • Perform data entry for all subject information into EDC databases as required
  • Perform peer review, quality review of all EDC data entered as required
  • Accountable for sending queries for clarity associated with incoming information if required
  • Contributes to safety and pharmacovigilance training programs.
  • Collaborates with Regulatory Affairs to ensure appropriate reporting of pharmacovigilance and drug safety information to regulatory agencies and prescriber community.
  • Administer Sitero Mentor Event Reporting system if needed
  • Participate in team calls and provide updates on issues noted at study sites

Essential Qualification and Experience:

  • Minimum 2+ year of experience of working in clinical trial domain
  • Degree in Life Science/Pharma or Equivalents

Professional Skills:

  • 2+ year of experience in clinical research domain
  • Awareness of GCP, GDPR HIPAA regulations
  • In depth Knowledge and understanding of clinical trials and its phases
  • Strong organizational, documentation, and interpersonal skills essential to interact with clients, management, peers and cross functional teams effectively.
  • Good working knowledge of US and EU drug safety regulations, CIOMS and ICH guidelines.
  • Excellent verbal, written and presentation skills.
  • Innovative, collaborative, initiative-taker.

Compensation and Benefits: Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits.


  • Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as needed.
  • Willing to work in shifts as and when needed.
Apply Now

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