Data Manager for Clinical Trials

Responsibilities

• Track database set-up, testing, maintenance, and data entry
• Communicate with clients, project teams, and vendors regarding data management matters
• Review study documents and develop project-specific guidelines and instructions
• Design eCRF, Data Management, and Data Validation Plans and test EDC databases
• Ensure data entry, follow-up, and validation, including manual CRF review and SAE reconciliation
• Code medical data and track metrics leading to database lock
• Coordinate the processing, dispatch, and archiving of CRFs and queries
• Maintain Clinical Data Management working files and perform database QC checks
• Train site staff and project teams on CRF completion and data management topics

Requirements

• College or University degree in Life Science (Pharmacy degree is a plus)
• Demonstrated experience managing clinical or medical data
• Full working proficiency in English
• Experience with Clinical Data Management systems such as Medidata Rave or Oracle InForm
• Proficiency in MS Office applications
• Strong organizational and time management skills
• Ability to work independently and multi-task

About the Company

PSI is a leading, privately owned Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originally founded in Switzerland, PSI provides full-service support for clinical trials globally. We are committed to delivering high-quality, timely services across a broad spectrum of therapeutic indications and foster an inclusive culture where diverse colleagues can thrive and contribute to groundbreaking pharmaceutical advancements.