Design and build eCRFs within Medidata Rave, ensuring adherence to protocol and data standards.
Develop and maintain comprehensive Data Management Plans.
Perform data validation and quality checks, resolving data discrepancies and queries.
Coordinate with clinical trial sites to ensure timely and accurate data entry.
Perform medical coding using MedDRA and WHO Drug dictionaries.
Qualifications:
Bachelors degree in Life Sciences or a related field.
0- 2+ years of experience in clinical data management.
Strong proficiency in Medidata Rave.
Excellent knowledge of GCP and 21 CFR Part 11.
Strong attention to detail and problem-solving skills.
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Employement Category:
Employement Type: Full timeIndustry: Pharma / BiotechRole Category: Bio Tech / R&D / ScientistFunctional Area: Not SpecifiedRole/Responsibilies: Clinical Data Management Job in CLIN