Latest Clinical Data Management Scientist (CDM) Scientist at Accenture, Interested and eligible candidates can check out all the details given the same below.
Job title: Clinical Data Management Scientist
Job Location: Bengaluru
About Company:
Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.
What would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings – Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes
by converging around the patient, connecting scientific expertise with unique insights into the patient experience. You will be working as a part of the Study Startup team which is responsible for Project Initiation, Planning, Implementation, Control & Evaluation and Close-Out activities which includes initiation of trial capacity, trial setup activities, etc. You will be expected to manage & review data generated through manual or programmed listings including, but not limited to all external data sources and SAEs.What are we looking for
• Adaptable and flexible
• Problem-solving skills
• Ability to work well in a team
• Ability to manage multiple stakeholders
Roles and Responsibilities for CDM Scientist at Accenture:
• In this role you are required to do analysis and solving of increasingly complex problems
• Your day to day interactions are with peers within Accenture
• You are likely to have some interaction with clients and/or Accenture management
• You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments
• Decisions that are made by you impact your own work and may impact the work of others
• In this role you would be an individual contributor and/or oversee a small work effort and/or team
• Please note that this role may require you to work in rotational shifts
Qualifications we seek in you for CDM Scientist at Accenture!
Bachelor of Pharmacy/BSc/Master of Pharmacy/MSc
Possible Interview Questions may be asked for CDM Scientist at Accenture
1. Can you describe your experience in clinical data management and your familiarity with regulatory guidelines and industry standards?
Answer: In my previous role as a Clinical Data Management Scientist, I have gained hands-on experience in managing clinical trial data. I am well-versed in regulatory guidelines, such as ICH-GCP and CDISC standards, which govern the collection, handling, and analysis of clinical data. I have worked with various electronic data capture (EDC) systems and have a strong understanding of data management processes, data cleaning, and data quality assurance.
2. How do you ensure the accuracy and integrity of clinical trial data throughout the data management process?
Answer: Ensuring the accuracy and integrity of clinical trial data is paramount. I employ rigorous data validation checks and implement comprehensive quality control measures at various stages of the data management process. I closely collaborate with cross-functional teams to develop data management plans, including data validation plans and edit check specifications. I perform thorough data review and reconciliation to identify and resolve any discrepancies or inconsistencies in the data.
3. Can you explain your experience with data cleaning and database lock activities?
Answer: I have extensive experience in data cleaning and database lock activities. I work closely with the study team to develop and execute data cleaning plans. I perform data query management, resolve data discrepancies, and ensure data completeness and consistency. I also participate in database lock activities, which involve finalizing the database for analysis and ensuring that all data queries have been resolved and data cleaning activities are completed according to the study timelines.
4. How do you handle challenges or issues that arise during the data management process, such as missing data or data discrepancies?
Answer: Challenges are an inherent part of the data management process, and I approach them by employing a proactive and solution-oriented mindset. When faced with missing data or data discrepancies, I investigate the root cause, collaborate with the relevant stakeholders, and propose appropriate corrective actions. I adhere to standard operating procedures and regulatory guidelines to address the challenges while maintaining data integrity and ensuring compliance.
5. How do you stay updated with the latest developments and advancements in clinical data management practices and technologies?
Answer: Staying updated with the latest developments in clinical data management is essential. I regularly participate in industry conferences, webinars, and workshops focused on data management best practices. I am a member of professional associations and online forums, allowing me to engage with peers and stay informed about emerging trends and advancements. I actively seek out training opportunities and continuously expand my knowledge base to incorporate the latest technologies and industry standards into my work.
