Marwa Ali
About Marwa Ali
Marwa Ali is a Submission Manager, Clinical Trials at Bristol Myers Squibb in Hillingdon, England, with extensive experience in clinical research and data analysis.
Current Role at Bristol Myers Squibb
Marwa Ali currently holds the role of Submission Manager, Clinical Trials at Bristol Myers Squibb in Hillingdon, England, United Kingdom. In this position, she oversees the management and submission processes for clinical trials. Her responsibilities likely include coordinating with various departments to ensure accurate and timely submissions while adhering to regulatory guidelines.
Professional Experience at Parexel
Marwa Ali has a rich history of employment at Parexel, where she held multiple roles from 2014 to 2021. She progressed through various positions such as Drug Safety Assistant, Clinical Trial Specialist I, and Senior Initiation Clinical Research Associate. Her roles at Parexel culminated in the position of Senior Initiation Clinical Research Associate, showcasing her growth and adaptability within the company. Marwa also served as the Sports & Social Club Secretary, reflecting her involvement in the corporate community.
Education and Qualifications
Marwa Ali earned her Bachelor's degree in Biomedical Sciences, General from Brunel University London, where she studied from 2008 to 2011. Her academic background in biomedical sciences provides a strong foundation for her roles in clinical research and trial management. Additionally, her participation as a Student Ambassador indicates her engagement during her university years.
Achievements in Clinical Research
Marwa Ali was a finalist in the Pharmatimes 2020 competition, highlighting her competence and recognition within the pharmaceuticals industry. This achievement underscores her expertise and commitment to excellence in clinical research and trials.
Skills and Expertise
Marwa Ali possesses significant skills in data analysis and clinical research, essential for her current and past roles. She is adept at using Microsoft Excel and Microsoft Word for various professional tasks, which aids in her ability to manage, analyze, and report data effectively. Her demonstrated history in the pharmaceuticals industry reflects her capability to deliver high-quality results in customer service and trial management.