Dr. Aslam T Abdulla, Pharmd Email & Phone Number

Saskatchewan, Canada

Victoria, British Columbia, Canada

• Worked for Novartis India as an external employee for the role of Clinical Scientific Expert• Ensured the delivery of high-quality clinical trial data insights and analysis in alignment with the Integrated Clinical Trial Team (iCTT) guidelines.• Conducted comprehensive clinical data reviews, identifying insights through patient-level analysis, trend identification, and supporting Interim Analysis, Database and Post Lock activities. Actively participated in resolving clinical data issues.• Collaborated cross-functionally with relevant departments to enhance the quality of clinical data reviews, with a focus on subject safety and eligibility, data integrity, trend identification, analysis, and remediation. Also, played a key role in identifying cases for medical review.• Contributed to the development of Data Review/Quality Plans (DRP/DQP) and data review strategies, ensuring consistent implementation of protocol-level deviations, eligibility criteria, and study assessments across the trial.• Worked in conjunction with the relevant line functions to assist in Case Report Form (CRF) development and supported the implementation of data capture tools.• Facilitated improvements in the data review process, such as identifying delinquent or redundant reports and introducing innovative data analysis processes and tools.• Collaborated with relevant line functions to develop study-level documents, including the clinical sections of essential regulatory documents such as Investigator’s Brochures, briefing books, safety updates, and submission dossiers.• Assisted in reviewing and writing clinical trial documents for study CSR activities and contributed to publications in coordination with relevant line functions.

Bengaluru Area, India

• Provided comprehensive monitoring support for end-to-end activities, encompassing the Study set-up phase, Conduct phase, and Close-out phase, to the project management team for designated studies. Ensured that all tasks were executed in accordance with service level agreements (SLAs) and within project timelines.• Maintained regular communication with internal and external Project leads, ensuring a seamless continuation of projects by sharing updates on activities performed.• Collaborated closely with Clinical Research Associates (CRAs), Clinical Monitors (CMs), and Clinical Leaders (CLs) on a daily basis. Clarified discrepancies and resolved Data clarification queries, employing validity checks to maintain a clean database.• Monitored and facilitated the timely release of patient laboratory reports by diligently following up on any pending activities with the related team(s).• Demonstrated strong analytical skills by performing Data revision and Data reconciliation, aiding in issue resolution and contributing to the timely database lock within the assigned time limits.• Actively participated in study team meetings and effectively implemented action items in coordination with regional and global project leads.• Served as the point of contact for assigned deliverables to Sponsors or project Stakeholders, including the preparation, handling, distribution, and archiving of study monitoring reports.

Bengaluru, Karnataka, India

• Took on a central role in managing multiple projects from sponsors, demonstrating strong project management skills and the ability to handle diverse responsibilities concurrently.• Provided essential lab data monitoring support, ensuring the integrity and accuracy of data. This involved sending out monthly reports, meticulously querying sites for data discrepancies, and maintaining regular monitoring of lab data for resulting and reporting.• Played a pivotal role in maintaining clear and effective communication channels with sponsors, ensuring alignment with project goals and objectives.• Demonstrated a keen eye for detail in the monitoring process, consistently identifying and addressing data discrepancies to uphold the quality and reliability of the study data.• Leveraged effective querying strategies to communicate with site teams, fostering collaboration and prompt resolution of datarelated issues.• Maintained a proactive approach to lab data monitoring, implementing preventive measures to mitigate potential data discrepancies and ensure the smooth progress of projects.• Collaborated with crossfunctional teams to streamline processes, contributing to increased efficiency and effectiveness in managing project deliverables.• Demonstrated a commitment to delivering highquality results, meeting project timelines, and exceeding sponsor expectations in lab data monitoring and reporting.

Bengaluru, Karnataka, India

• Provided comprehensive lab data monitoring support for assigned studies, ensuring the accuracy and reliability of data.• Conducted regular monitoring of lab data, addressing discrepancies promptly to maintain data integrity.• Executed data entry tasks with precision and attention to detail as an integral part of the overall data monitoring process.• Managed and entered data into relevant systems, maintaining a high standard of accuracy and completeness.• Demonstrated a proactive approach in identifying and resolving issues, contributing to the overall success of the assigned studies.• Collaborated effectively with cross-functional teams to streamline processes and enhance the efficiency of lab data monitoring, including data entry tasks.• Maintained a commitment to delivering high-quality results within specified timelines, meeting or exceeding study requirements.

Coimbatore Area, India

• Completed a rigorous internship in a hospital accumulating 1 year of hands-on experience, which involved working in a pharmacy, patient counseling, and drug information center.• Gained valuable insights during an 80-hour stint at a community pharmacy, developing a deep understanding of community pharmacy operations.• Actively contributed to the healthcare team by providing crucial disease and drug information in a timely manner. This information included insights on common disease conditions in the ward, precise drug dosing recommendations, potential drug interactions, side effects, and contraindications.• Collaborated with the medical team to ensure that healthcare professionals had access to up-to-date and accurate information, enabling them to make informed decisions about patient care and medication management.• Continuously demonstrated a commitment to patient safety and well-being by offering essential counseling services, empowering patients to better understand and adhere to their prescribed medication regimens.• Assisted in optimizing patient outcomes through the provision of expert guidance on medication selection and usage, taking into consideration individual patient profiles and medical histories.• Showcased strong communication and interpersonal skills while working directly with patients and healthcare professionals, fostering a positive and collaborative healthcare environment

Health Informatics, Health Information/Medical Records Technology/Technician, 4.0

Data Management: Proficient in collecting, analyzing, and interpreting health data sets to address organizational needs. Experienced.

Doctor Of Pharmacy - Pharmd, Clinical, Hospital, And Managed Care Pharmacy