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If interested in applying for this position, please send your resumes to careers@sciformix.com
Process Associate, Pharmacovigilance
Responsibilities:
Skills Required:
Execute drug safety data management processes (case entry, medical coding, safety narrative writing, QC, medical review, PSUR scheduling, aggregate report writing, etc.)
Ensure delivery of services meets or exceeds service level agreements
Ensure operational compliance with applicable regulatory requirements

Implement process & productivity continuous improvement techniques to improve operational efficiency
Quality of data

1-2 years of hands on pharmaceutical product development (one of formulation development, PK studies, Phase IV studies, regulatory affairs etc)

Formal training/certification in pharmaceutical product development (B. Pharm., M. Pharm., M. Sc.., in life sciences)
Good oral and written communication skills
Understanding of global regulatory requirements
Ability to work independently with minimal supervision, yet should be a good team player
Knowledge of IT tools used in scientific data management, such as Oracle AERS, Relsys, ArisG, SAS, or others.
 
 
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