Rahul Jain

About Rahul Jain

With over 12 years of diverse corporate experience, I have developed a strong foundation in Clinical Data Management (CDM), encompassing various facets of clinical trial execution and data handling.In my career, I have acquired hands-on expertise in orchestrating the setup, conduct, and close-out activities of clinical developments across all phases, including Phase I, Phase II, and Phase trials. My role extends beyond mere execution, as I actively engage with internal and external stakeholders, providing training to new associates, offering valuable insights for process enhancements, and serving as the primary contact for the targeted source data verification (tSDV) process across teams.Notably, I played a pivotal role in setting up the inaugural trial utilizing the \"DO Accelerate\" tool, a groundbreaking initiative within the industry. Additionally, my contributions to the User Acceptance Testing (UAT) of the UAT ME tool underscore my commitment to leveraging technology for streamlined data management practices.Collaboration and knowledge-sharing are integral aspects of my approach, fostering a culture of continuous learning and improvement. I possess extensive experience in drafting various trial documents, including edit check specs, study specifications, and CRF completion guidelines.My proficiency extends to working with an array of platforms such as Inform, RAVE, and eTMF Veeva Vault, among others. Furthermore, my team management experiences and client interaction skills have equipped me with the ability to navigate complex projects and deliver results effectively.With a deep understanding of the clinical research and drug development process, I bring to the table an in-depth comprehension of clinical data management processes across diverse therapeutic areas, including oncology and neurology.Moreover, my tenure includes over 2 years of experience in report writing for under-development drug candidates, wherein I oversaw a team of 4 individuals and spearheaded the implementation of a quality check framework, ensuring accuracy and excellence in our deliverables.

Experience

1. Senior Global Data Manager

   Johnson & Johnson Innovative Medicine

   Nov 2024 — Present · Hyderabad, IN

Education

• Excellence H.S. School Sagar, Madhyapradesh

  Higher Secondary, Biology/Biological Sciences, General

  1998 — 2005

Skills

• Risk Based Moniotoring
• Toxicology
• Pharmacology
• Pipeline Analysis
• Medical Writing
• Drug Discovery
• Clinical Data Management
• Secondary Research
• Pharmacovigilance
• Rave
• Molecular Modeling
• Insight Generation
• Clinical Trials
• Inform
• Competitive Intelligence
• Electronic Data Capture (Edc)
• Regulatory Affairs
• Market Research
• Databases