Technical Product Manager - Clinical Data Management System

March 8

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Logo of Alimentiv

Alimentiv

Alimentiv is a specialty contract research organization focused on gastrointestinal (GI) and liver diseases. With over 30 years of experience, Alimentiv offers a comprehensive range of clinical research and imaging services, including clinical trial management, site management, regulatory affairs, and precision medicine. The company is at the forefront of medical research and development, providing state-of-the-art imaging solutions and actionable biomarker insights. Alimentiv supports the development of GI compounds and is active in more than 60 countries, working with a network of medical and operational experts to accelerate clinical trials and patient recruitment.

Clinical Trials Design • Planning • Safety Management • Custom Services • Study Management

📋 Description

• We are seeking a highly skilled Product Manager to lead the development and enhancement of our innovative Clinical Data Management System (CDMS) for Medical Imaging in clinical trials. • The ideal candidate will have a strong technical background in Computer Science or Engineering, complemented by a deep understanding of Medical Imaging and Clinical Trials. • This role requires a product-centric approach, with the ability to drive strategic product decisions that align with business objectives, industry trends, and customer needs. • As a Product Manager you will be responsible for defining and executing product strategies, managing the product lifecycle, and collaborating with cross-functional teams to deliver effective solutions. • You will lead a cross functional product team of clinical and software development specialists to ensure our products meet evolving corporate, industry, customer, and regulatory requirements. • If you are passionate about leveraging technology to advance medical imaging in clinical trials, we invite you to join our team and contribute to setting new standards in this field.

🎯 Requirements

• Minimum requirement: Bachelor's degree with 4-6 years related experience; excellent communication skills and experience in stakeholder management • Preferred: Master's degree + 7-9 years related experience • Deep technical knowledge and experience with software development, artificial intelligence, machine learning, programming, software as medical device (SaMD) regulations and standards • Prior experience in product strategy and roadmap development in the clinical research field; understanding of regulatory and compliance standards associated with clinical trials • Background in software engineering/development • Vendor management experience

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