Job Description
SKILLS
• Min 5 yrs of experience in Data Acquisition domain.
• 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).
#LI-REMOTE
• Min 5 yrs of experience in Data Acquisition domain.
• 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).
#LI-REMOTE
💡 Quick Summary
Seeking a career-building opportunity? The Data Manager - Lead position is now open for candidates interested in the Database Administrator sector. This role in New Delhi offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Database Administrator is a plus.
