Clinical Data Management Trends, Tools & Career Pathways Webinar Conducted Successfully By Biotecnika
- Date: March 7, 2025
- Time: 7 PM – 8 PM IST
- Venue: YouTube LIVE
In today’s rapidly evolving healthcare and pharmaceutical landscape, Clinical Data Management (CDM) plays a crucial role in ensuring the integrity, accuracy, and compliance of clinical trial data. To shed light on the latest trends, tools, and career opportunities in CDM, BioTecNika hosted an insightful webinar on March 7, 2025, featuring two esteemed industry experts: Shweta Birajdar, Clinical Data Management Scientist at BioTecNika, and Priyanka Lakde, Manager, Clinical Data Coding at Sun Pharmaceuticals.
This engaging session provided attendees with a comprehensive understanding of CDM and its significance in clinical research. The speakers explored key data management processes, including data collection, validation, and cleaning, highlighting how technology and automation are transforming the field. Participants gained valuable insights into cutting-edge tools, emerging industry trends, and the evolving job market for clinical data professionals.
A key focus of the webinar was career growth in CDM, where industry experts outlined the skills in demand, job roles, and pathways to success in this high-growth domain. From understanding regulatory requirements to mastering advanced software solutions, attendees received actionable insights into how they can build a thriving career in clinical data management.
The interactive Q&A session allowed participants to engage directly with the experts, addressing their queries on clinical data compliance, job prospects, and industry advancements. The session concluded with a roadmap for aspiring professionals to kick-start their careers in CDM, along with information on upcoming training programs and industry events. With CDM becoming an indispensable part of modern clinical research, this webinar served as a valuable learning experience for students, professionals, and researchers eager to excel in the field.
The webinar showcased an esteemed lineup of speakers:
Priyanka Lakde
Clinical Research & Regulatory Affairs Expert
Priyanka Lakde led an engaging discussion on the latest trends and advancements in Clinical Data Management. She highlighted the evolution of CDM practices driven by emerging technologies such as artificial intelligence (AI), machine learning (ML), and cloud-based data management solutions. Her session emphasized the growing need for efficient data handling, automation, and real-time analytics to improve the accuracy and reliability of clinical trial outcomes.
In addition to technological advancements, Priyanka explored career growth opportunities in CDM, shedding light on the various job roles available in the industry, including Clinical Data Coordinators, Data Managers, and CDM Specialists. She provided attendees with a roadmap to acquire essential skills, certifications, and industry-relevant expertise to build a successful career in this dynamic field.
Shweta Birajdar
Clinical Data Management Scientist, Biotecnika
Shweta Birajdar provided a deep dive into the key components of Clinical Data Management, outlining the essential processes of data collection, validation, and cleaning. She emphasized the significance of data accuracy, integrity, and compliance in ensuring the success of clinical trials.
Her session also covered the role of technology and automation in CDM, highlighting how AI-driven solutions, electronic data capture (EDC) systems, and cloud-based platforms are transforming the way clinical data is managed. Additionally, she discussed industry standards and regulatory compliance frameworks such as Good Clinical Practice (GCP) guidelines, FDA regulations, and CDISC standards, ensuring that attendees understood the importance of regulatory adherence in clinical research.
The insightful discussions by both speakers provided a comprehensive overview of Clinical Data Management, equipping attendees with knowledge of emerging technologies, industry trends, and career pathways in the field.
Key Insights from the Webinar
- Technology is Transforming CDM – AI, machine learning, and automation enhance data accuracy, streamline workflows, and improve decision-making in clinical trials.
- Data Quality is Critical – Ensuring data integrity, validation, and compliance is essential for reliable clinical research outcomes.
- High Demand for CDM Professionals – Roles like Clinical Data Coordinator and CDM Specialist are in demand, offering strong career growth.
- Regulatory Compliance is Essential – Adhering to GCP, FDA guidelines, and CDISC standards ensures ethical and secure data management.
- Future of CDM: Automation & AI – AI-driven analytics, cloud-based management, and electronic data capture (EDC) are revolutionizing the field.
The webinar provided valuable insights into CDM trends, essential skills, and career opportunities, guiding attendees toward a successful career in this field.
Esteemed Speakers
The webinar on “Clinical Data Management: Trends, Tools & Career Pathways” featured a distinguished panel of industry experts who shared their insights and expertise on the evolving landscape of Clinical Data Management (CDM).
Table of Contents
Priyanka Lakde
Clinical Research & Regulatory Affairs Expert
With over 13 years of experience in clinical research and regulatory affairs, Priyanka Lakde is a highly respected professional in the pharmaceutical industry. She holds a Master’s degree in Clinical Research and Regulatory Affairs and has contributed significantly to clinical data management, regulatory compliance, and clinical trial execution. Her career includes pivotal roles at Cognizant, IQVIA, Syneos Health, and her current position as Manager, Clinical Data Coding in the Global Clinical Development Department at Sun Pharmaceuticals.
Priyanka’s expertise spans clinical data quality assurance, global regulatory standards, and pharmaceutical research & development. She is committed to optimizing data integrity, streamlining research processes, and ensuring compliance in clinical studies. Her contributions have been instrumental in maintaining high-quality standards in clinical research and fostering innovation within the industry.
Shweta Birajdar
Clinical Data Management Scientist, BioTecNika
Worked at TCS, Aston Carter, and EVERSANA
Shweta Birajdar, an expert in clinical data management, regulatory affairs, and drug safety, has contributed significantly to leading organizations like TCS, Aston Carter, and EVERSANA. She has ensured GCP compliance data quality and optimized clinical trial systems. As a Regulatory Affairs Specialist Manager in Jeddah, she led a team of 29 professionals, overseeing compliance and technical documentation.
Her expertise in market research, regulatory reporting, and training has strengthened her role as a mentor in clinical research. With a strong background in data validation, audit readiness, and adverse event processing, Shweta continues to drive excellence in clinical and regulatory sciences. Both speakers shared valuable insights, career guidance, and a deeper understanding of CDM’s role in clinical research.
About BioTecNika
With 18+ years of expertise, BioTecNika is India’s No.1 biosciences platform, connecting 4.5M+ professionals worldwide. We specialize in education, recruitment, and talent development for the biotech and pharma industries, helping individuals and organizations stay ahead in the ever-evolving world of life sciences. At BioTecNika, we are committed to empowering careers, fostering innovation, and shaping the future of biosciences.
