Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences
Pfizer · India - Chennai · Global
Clinical Data Science
–
Not yet analysed
Demand72
Career growth68
Healthcare fit78
Remote potential55
5-year outlook
Likely a competitive pharma clinical data sciences role with progression toward clinical monitoring, risk-based monitoring, or clinical data science leadership. Exact compensation is not specified in the posting.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
–
Date found
2026-10-29
Intelligence details
Why this is worth applying to
Worth considering for clinicians who want to move into pharma clinical data oversight and centralized monitoring. Less suitable for those seeking patient-facing work or without any clinical trial/data-review exposure.
Who should apply
Physicians, nurses, pharmacists, IMGs, and healthcare graduates with exposure to clinical trials, protocol review, safety reporting, data review, or CRO/pharma operations.
CV angle
Frame real clinical experience around protocol adherence, adverse event recognition, data quality review, safety signal interpretation, risk assessment, and cross-functional collaboration. Emphasize any clinical trial, research, GCP, or data-review exposure without overstating non-clinical experience.
Skills to highlight
- Clinical data review
- Risk-based monitoring
- Clinical trial operations
- Adverse event and safety signal recognition
- Good Clinical Practice (GCP)
- Data quality and surveillance
- Cross-functional collaboration
- Attention to detail
Role summary
A pharma clinical data sciences role focused on centralized monitoring and surveillance of clinical trial data, likely supporting data review, risk identification, and trial oversight rather than direct patient care.
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