Your Competencies: Review many hundreds to thousands of clinical trials data to form the metadata based data mining rules to search targeted domains and variables.
Your Competencies: Review many hundreds to thousands of clinical trials data to form the metadata based data mining rules to search targeted domains and variables.
Programming of data mining rules and output the metadata results
Review and format the raw data extracted for hundreds to thousands of clinical trial studies of target domain
Standardize the unique values of raw data of target variables matching controlled terminologies Perform QC of the standardized data for hundreds of studies by programming
Create concise summary report of the QC findings to refine the data mining rules as necessary Attends team meetings with proactive interaction with stakeholders across the functional areas Create documentation of the programs and work done
Education & Experience: Bachelor’s or Master’s degree in life science or related field
Having 6 or more years of experience working with raw clinical and medical data collected in clinical trials, in a pharmaceutical or clinical research setting for multiple sponsors data
Knowledge of eCRF and study design in the Clinical Database Systems like Rave, Inform, Oracle RDC etc
Experience in SDTM standards and NCI controlled terminologies
Programming experience, preferably in SAS
Good documentation, communication, analytical and interpersonal skills
Ability to work independently and as part of a team to adhere to deadlines Prefer experience in oncology trials