To Ensure integrity of clinical trial database.
Perform Data Validation ensuring completeness and clean data.
Ensure availability of data to relevant stakeholders.
Write, send, update, and resolve data clarifications.
Create test cases and test validation procedures.
Perform UAT of the database.
Generate reports and communicate with stake holders in a timely manner
Understand and comply with all applicable standard operating procedures and working instructions.
Develop and maintain good communications and working relationships with Data Management team.
Assist in timely scanning, book marking and indexing of documents in novoDOCS
Ensure good documentation practices are followed.
Qualifications
Masters or Bachelor degree in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science orclinical information management or equivalent qualifications.
The candidate should have around 6 to 7 years of data management experience and the majority of this within Pharmaceutical Industry or Development.