Haseeb M. Ms,R Ph
About Haseeb M. Ms,R Ph
Haseeb M. Ms, R Ph is a Safety Records Associate at BeiGene with a background in drug safety and clinical data analysis, previously working at The Janssen Pharmaceutical Companies of Johnson & Johnson, CData Systems, and inVentiv Health Clinical.
Current Position at BeiGene
Haseeb M. currently holds the position of Safety Records Associate at BeiGene. His responsibilities include overseeing safety databases, ensuring timely processing of Individual Case Safety Reports (ICSRs), and contributing to the development of compliance targets. Additionally, Haseeb supports ongoing continuous improvement and quality control measures, including CAPA investigations and implementation of corrective actions.
Previous Roles and Experience
Haseeb M. has worked in several roles throughout his career, showcasing a diverse skill set in the pharmaceutical industry. He spent four years at The Janssen Pharmaceutical Companies of Johnson & Johnson as a Drug Safety Associate in Cherry Hill, NJ, where he honed his skills in safety report processing and compliance. Earlier in 2017, he worked briefly at CData Systems as a Clinical Data Analyst in East Windsor, NJ for two months. In the same year, he also worked at inVentiv Health Clinical as a GSPV Associate for six months in Ann Arbor, MI. He started his professional journey at CData Systems as a Clinical Data Analyst Trainee from 2016 to 2017.
Educational Background
Haseeb M. achieved a Master's degree from Northeastern Illinois University, where he studied from 2015 to 2016. This educational foundation has played a crucial role in equipping him with the knowledge and skills required for his various roles in the pharmaceutical and healthcare industries.
Specific Contributions and Initiatives
Throughout his career, Haseeb M. has contributed to the development and improvement of several processes and systems. He has been involved in the creation of novel Individual Case Safety Report (ICSR) book-in processes and supported daily safety database workflows. His work ensured ICSRs were processed according to internal timelines and involved periodic reconciliation from various non-clinical trial sources. Additionally, Haseeb has contributed to inspection readiness activities, supported audits and inspections, and managed relationships with vendors and business partners through Pharmacovigilance Agreement reviews.
Support to Adjacent Teams
Haseeb M. has continuously provided extensive cross-functional support to adjacent teams, ensuring both the timely book-in of Adverse Event (AE) reports and maintaining process compliance. His collaborative approach has facilitated seamless operations within his teams and contributed to achieving organizational goals effectively.