Clinical Data Management Scientist

Skill required: Clinical Data Operations - Clinical Data Management
Designation: Clinical Data Management Scientist
Qualifications:Bachelor Degree in Life Sciences,Master Degree in Life Sciences
Years of Experience:5 to 8 years

Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Songall powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries.
What would you do You will be aligned with our Life Sciences RD 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 and enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Clinical Data Operations involves the management and oversight of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure accuracy and compliance with regulatory standards. The goal is to support clinical research by providing high-quality data that can be used to evaluate the safety and efficacy of medical treatments.A critical phase in clinical research that assures collection, integration and availability of data at appropriate quality and cost. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH).The Clinical Data Manager is responsible for end-to-end data management activities across clinical trials, ensuring high-quality, reliable, and regulatory-compliant clinical data to support study objectives and regulatory submissions.Key Responsibilities:Study Setup Start-up, Study Conduct and Study Close-out with Stakeholder Management and Compliance Quality
What are we looking for Ability to establish strong client relationshipAbility to manage multiple stakeholdersAbility to meet deadlinesAbility to perform under pressureAbility to work well in a teamHands-on experience with EDC systems (Medidata Rave, Inform, Veeva, etc.)Exposure to data visualization/reporting tools and ExcelKnowledge of coding dictionaries (MedDRA, WHO-DD)
Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problemsYour day to day interactions are with peers within AccentureYou are likely to have some interaction with clients and/or Accenture managementYou will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignmentsDecisions that are made by you impact your own work and may impact the work of othersIn this role you would be an individual contributor and/or oversee a small work effort and/or teamPlease note that this role may require you to work in rotational shifts


Qualification
Bachelor Degree in Life Sciences,Master Degree in Life Sciences