This is a fully remote position, open to applicants in Hungary, +3 more countries.

📋 Description

• Development and execution of solutions addressing global technical service challenges related to the EDC tool Medidata RAVE.

• Accountable for designing the electronic Case Report Form (eCRF) within the leading EDC Rave system.

• Tasked with preparing and/or reviewing draft and final versions of eCRFs and edit check specifications for assigned projects to ensure quality and consistency.

• Maintain a detail-oriented approach while participating in sponsor meetings and audits/inspections.

• Assist Managers in gathering data for productivity, quality, timelines, and resource planning.

• Responsible for executing quality control procedures during specification development.

• Conduct team meetings and offer guidance to Programmers and Data Managers.

• Engage in the validation of EDC studies upon request.

• Oversee the creation and maintenance of library objects within the Global Libraries.

• Ensure compliance with standard object usage across the organization.

• Carry out all tasks related to specification development for study build and database design in accordance with standard procedures.

⛳️ Requirements

• A minimum of 5 years of relevant experience, including data management and/or database programming and specification design activities.

• Must be a Medidata Rave EDC Certified Study Builder.

• Strong understanding of the drug development process and Clinical Data Management Programming.

• Previous experience with protocol interpretation and building/programming databases in RAVE.

• Candidates must possess fluency in the English language, both spoken and written.

🏝️ Benefits

• Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, and remote working allowances.

• A genuine commitment to work-life balance.

• Flexibility in working hours.

• Comprehensive onboarding process supported by a personal mentor.