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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Data Acquisition Specialist

Job ID R0000028896 , India

SKILLS

● Able to understand complex interdependencies.
● Communicate independently, proactively and clearly to internal and external stakeholders, able to work autonomously on the non-CRF data strategy for the study team.Take ownership of non-CRF data.
● Identify risks and suggest mitigation plans.
● Influence the study team to adhere to (non-CRF principles) and processes, speak up and challenge where necessary.
● Negotiate contingency plans to mitigate delays of deliverables.
● Can demonstrate curiosity for data and be able to learn fast and think smart.
● Scientific background in at least one of the following: medical, biological, lab, imaging, life sciences.
● Comfortable with working across multiple platforms and tools.
● Experience of clinical trials.

TASKS

● Leads the collection of non-CRF data, during study set-up, conduct and close out activities for multiple studies, contributing to fit for purpose data quality.Including IxRS data loaded into the eCRF.
● Close collaboration with the non-CRF vendors/data providers to set up data transfer agreements and ensure timely and quality non-CRF data delivery.Come to mutual agreements and intelligently negotiate with the vendor and study team to be able to deliver what the study needs.
● Selects and implements appropriate study conventions including non-CRF data collection standards, processes, knowledge sharing and best practices on assigned study(s).
● Proactively develops study level project plans (including contingency plans) to ensure timely delivery of quality non-CRF study data to support project milestones.
● Represents DSD on Study working groups or sub-teams and works with the study team to develop and implement specifications and processes related to non-CRF vendors/data providers.
● Effectively communicates non-CRF data collection deliverables, status of work and data issues to the DQL and other study team members.Coordinates cross-functional non-CRF tasks with strong understanding of downstream processes and stakeholder needs and impacts.
● Identifies the need for new processes and guidance documents.
● In-depth understanding of the business of his or her discipline and the wider DSD organization.
● Understand the conceptual basis for data management conventions, standards and processes.
● Good understanding of the role of data management, biostatistics, statistical programming and the study team in the drug development process.
●Understands compliance, regulatory principles and follow GxP requirements (SOPs, Policies etc).

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