FAZAL UDDIN MOHAMMED

Clarivate Analytics

Hyderabad

11.2013 - Current

To analyze clinical trial information through primary and secondary research, followed by collating clinical information from various sources, e.g. ClinicalTrials.gov and various clinical trial registries (Eudract, UMIN, ANZCTR, Japic, Chictr), company websites, annual reports, scientific journals, articles from PubMed, meeting reports, and biological conferences.
Provide all-around information on the latest drugs and medical devices, and write summaries of the results published from multiple sources.
Provide pharmaceutical competitive intelligence useful in drug discovery, sponsoring, and collaborating on clinical trials, and incurring approvals from regulatory authorities (FDA, EMA, Japanese MHLW).
Identification, assessment, and sourcing of intelligence data from internal and external sources.
Clinical trial data curation within the current internal dynamic processing guidelines.
Reviewed and edited internal guidelines for clarity and consistency.
Assisted in training new team members on content standards and tools.
Performing a quality check (QC) of data edited by fellow editors.
Ensure coverage of all major therapeutic areas, including oncology, cell therapy, biologicals, and rare diseases.
Provide patient segmentation information to enhance the growing field of personalized and precision medicine.
To identify areas of improvement and provide recommendations.

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