Job Description APPLY
Provide timely and professional ongoing management of clinical trial data by identifying and resolving errors and inconsistencies in eCRF data to ensure consistently high standard database(s) with respect to cost, quality and timelines.
1.Provide professional DM input on Clinical Trial Team(s)Review of clinical trial database design including User Acceptance Testing (UAT)
2.Responsible for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes chairing the meeting, writing the study specific validation checks and necessary reports to ensure high quality and consistent data.
3.Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks.
4.Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design.
5.Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), electronic or paper.
Experience: 3+ years
Job Location: Hyderabad
Salary:
Not Disclosed by Recruiter
Industry:
Pharma / Biotech / Clinical Research
Functional Area:
Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category:
R&D
Role:
Clinical Research Manager
Keyskills:
clinical dataclinical databaseclinical Oracle Clinical
Desired Candidate Profile
Education:
UG - B.Sc - Any Specialization, MBBS - Medicine, B.Pharma - Pharmacy
PG - Any Postgraduate - Any Specialization
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
PG - Any Postgraduate - Any Specialization
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
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