Associate Clinical Data Manager

IQVIA AG seeks an Associate Clinical Data Manager in Switzerland to lead data management projects, ensure data quality, and coordinate with stakeholders throughout the clinical research lifecycle.

The company is looking for a professional to act as the lead data manager for various projects, ensuring efficient and high-quality deliverables that meet sponsor requirements. This role involves coordinating with internal departments, external sites, and sponsors to support the overall clinical research process.

Responsibilities

• Collaborate with stakeholders to define study setup requirements.
• Execute database setup and validation to guarantee quality study design.
• Assist in validating new device integrations.
• Conduct regular data cleaning to ensure timely and high-quality deliverables.
• Maintain expected quality standards and meet customer expectations for all outputs.
• Provide training support for new team members.
• Lead internal study meetings, audits, and kick-off sessions with sponsors.
• Monitor project progress, identify risks, and implement corrective actions.
• Manage the development and implementation of new technologies or database revisions.
• Partner with programming teams to drive process innovation and automation.
• Review and advise on the creation, revision, and maintenance of core operating procedures.

Requirements

• Master's degree in Post Graduate Science or Bachelor's in Pharmacy, or equivalent qualification.
• Fluent spoken and written English.
• Advanced proficiency in Microsoft Excel, Word, and email management tools.
• Strong understanding of the drug development lifecycle and clinical research processes.