Clinical Data Svs Specialist Full Time NEW

Designation: Clinical Data Svs Specialist

Qualifications:Master of Pharmacy

Years of Experience:7 to 11 years

About Accenture

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 784,000 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.Visit us at www.accenture.com

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. Clinical Data Services involve the management and processing of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure the data is accurate and reliable. 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. These services are essential for regulatory compliance and successful trial outcomes. They often utilize specialized software and systems to manage the data efficiently. 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).

What are we looking for?

• Ability to establish strong client relationship
• Ability to handle disputes
• Ability to manage multiple stakeholders
• Ability to meet deadlines
• Ability to perform under pressure Roles and Responsibilities: Overall 7+ years of experience with exposure to Medidata RAVE EDC platform preferred. o Expertise in project management across Start-up, Conduct and Close out phases. o Manage delivery of projects through full data management study life cycle (Start-up, Conduct and Close out phases). o Excellent organizational, communication, and data management skills (detail oriented). o Must have skills for Microsoft Office tools like Excel, Word, and PowerPoint. o Knowledge of ICH, GCP, and other regulatory guidance as applicable to management of clinical documentation. o Ability to work in an extremely fast-paced environment with changing priorities. o Ability to work collaboratively and cross-functionally. o Attention to detail with problem-solving and analytical skills.