We\xe2\x80\x99re on a mission to change the future of clinical research. At Calyx, we help the biopharmaceutical industry bring medical treatments to the market, faster. Our mission is to change the world but to do this, we need people like you.
Apart from job satisfaction, we can offer you: HEALTH:
Medical plan for you and your dependents.
Personal Accident Insurance
Life Insurance
Critical illness cover
WEALTH:
Salary structure and Flexi basket
Provident fund of 12%
Gratuity scheme
YOURSELF: Internal growth and development programs & trainings
Data Analyst works closely with Scientific Lead under close guidance and supervision of their Line Manager to perform activities assigned in the project. Further responsibilities shall include support Data Management and Analytics team in data cleaning, data review, generation of quality outlier/data reconciliation and other custom reports. All tasks should be performed in accordance to corporate quality standards, SOPs/Work Instructions/Guidelines, ICH-GCP and/or other international regulatory requirements.
Accountability:
The Data Analyst will assist Scientific Lead in performing quality review
Assist Data Management and Analytics team in generation of Data Reconciliation, Quality Outlier, Custom Reports and reviewer performance metrics
Provide support in preparation of project specific reviewer performance report (as needed)
Assist in requirement gathering, testing and validation of Data Management applications
May assist Scientific Lead in identifying additional QC checks and setting up of data QC document
May assist Project Manager in setting up the data reconciliation and data QC documents
Skills:
Evidence of logical reasoning and structured problem-solving skills
Analytical thinking, methodical in delivering work activities (attention to detail) with first time quality
Time management and prioritization skills to meet objectives and timelines
Ability to work collaboratively within a team environment
Good interpersonal, oral and written communication skills
Learning ability and knowledge sharing approach; swift understanding of technologies and new processes
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Knowledge and Experience:
Minimum of 1 years work experience in clinical trials or in a relevant project management support role
Experience in medical imaging and/or clinical research industry
Evidence of technical aptitude with awareness/potential prior experience in Microsoft Office Products (basic computer skills).
Basic understanding/willingness to learn relevant ICH-GCP Guidelines, local regulatory requirements and Calyx SOPs and study specific procedures
Education:
Bachelor\'s Degree in a technical discipline (Math, Science, Engineering, Computing, etc.) or a related study, or equivalent project-related experience
Come as you are. We\'re proud to be a Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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