Licensing Project Manager

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Suvoda

WebsiteLinkedInAll Job Openings

501 - 1000 employees

⚕️ Healthcare Insurance

💊 Pharmaceuticals

☁️ SaaS

💰 $40M Venture Round on 2019-12

Healthcare Insurance • Pharmaceuticals • SaaS

Suvoda is a company specializing in delivering cutting-edge software solutions for managing complex clinical trials. It offers a single platform with products such as eConsent, Interactive Response Technology (IRT), electronic Clinical Outcome Assessment (eCOA), and ePatient, designed to streamline and enhance the efficiency of life-sustaining clinical studies, especially those in therapeutic areas like oncology and rare diseases. With their technology, they aim to provide full command over time-sensitive patient interactions and assist clinical trials in handling infinite variables and constant changes, ensuring high standards and effective patient consent management across various age groups to improve trial outcomes. Suvoda emphasizes collaboration with clients throughout the lifespan of a trial to maintain quality and success.

📋 Description

• Manage communication between Suvoda’s internal eCOA teams and instrument developers/license holders for questionnaires; • Manage communication between Suvoda’s internal Technical Solutions and Design teams and 3rd party translation vendors regarding development needs and client translation requirements; • Research license, translation, and eCOA requirements including layout, formatting, and appearance on devices. Determine the license holder is and how to get in contact; • Take ownership over the development of information gathering form to be collected at project outset to assist in license research; • Communicate and implement all translation and eCOA requirements, and timelines to correct internal eCOA teams; • Design, manage and update internal reference master guide as needed with license holder requirements for future reference; • Coordinate license holder reviews, as needed; • Supply translation vendor with English .json files and screen reports for translation; • Receive translated .json files from translation vendor and provide to the Technical Solutions team for implementation; • Create screen report documents for each questionnaire by copying and pasting individual screenshot images of each question for a particular questionnaire. The individual screenshot images will be generated by the Technical Solutions team; • Perform a basic proofread of the screen report documents to ensure all required screen content is present and in the correct order; • Coordinate revisions to the screen report documents and .json files between the Technical Solutions team and translation vendor, as needed; • Collaborate with Lead Project Managers regarding translation timelines in order for Lead Project Managers to communicate this information to the client;

🎯 Requirements

• 2-3 years of experience in pharmaceutical industry; • Strong licensing experience; • Bachelor’s degree required; • Strong interest in language, research and desire to join the pharmaceutical industry; • Experience in management of multiple simultaneous projects; • Ability to multitask; • Strong organization and detail orientation skills; • Self-motivated; • Professional communication skills;

🏖️ Benefits

• Health insurance • Retirement plans • Paid time off • Flexible work arrangements