Alira Health is a global consulting firm that partners with life sciences companies to develop innovative solutions in healthcare. The company specializes in a wide range of services including research and clinical development, regulatory compliance, and management consulting. Alira Health focuses on patient engagement, market access, and providing real-world solutions to improve patient outcomes. They are committed to environmental sustainability and actively participate in community involvement and ESG initiatives. Alira Health also provides technology solutions with a focus on improving life sciences research through empathy and scientific excellence.
Nuclear medicine • Rare disease • Lupus • Myasthenia gravis • Robotics
April 3
Alira Health is a global consulting firm that partners with life sciences companies to develop innovative solutions in healthcare. The company specializes in a wide range of services including research and clinical development, regulatory compliance, and management consulting. Alira Health focuses on patient engagement, market access, and providing real-world solutions to improve patient outcomes. They are committed to environmental sustainability and actively participate in community involvement and ESG initiatives. Alira Health also provides technology solutions with a focus on improving life sciences research through empathy and scientific excellence.
Nuclear medicine • Rare disease • Lupus • Myasthenia gravis • Robotics
• ensure DM tasks for the assigned studies are performed on time and within budget • partners with Sponsors, clinical and statistics to develop the data collection specification • manage in-stream data flow activities and deliver a quality database • leads and drives the DM team and acts as the reference point for the Sponsor • accountable for driving achievements of project milestones • provide Data Management input into the protocol • design the Case Record Form and guide process for CRF approval • define and develop the Data Management Plan, Data Validation Plan and their annexes • validation of the database and computerized checks • define the User Acceptance Test Plan (UAT) and execute the test activities • prepare CRF completion guidelines and train data-entry staff • query management and data cleaning process • create and test import programs for electronic data • run and monitor study data progress reports • lead the DM team and coordinate other DM staff
• Degree in life science, pharmaceutical, biology or related field or at least 3 years’ experience in data management field or similar in a pharmaceutical environment or equivalent • Knowledge of Data Management processes • Good Knowledge of pharmaceutical industry guidelines like ICH, GCP etc • Good Knowledge of coding dictionaries like MedDRA and WHO-DD or equivalent • Good Knowledge in one or more DM systems
• professional development • global travel • flexible work programs
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