Site Network Manager

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Alimentiv

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2020

⚕️ Healthcare Insurance

🔬 Science

💊 Pharmaceuticals

Healthcare Insurance • Science • Pharmaceuticals

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.

📋 Description

• Drive and deliver on the Alimentiv Site Network (ASN) Strategy. • Manage the identification, outreach, recruitment and onboarding of high quality, high performing sites into the North America ASN. • Develop strong relationships with high priority sites & partners through virtual or face-to-face meetings and conference attendance (travel required). • Build a deep understanding of the challenges of clinical research for sites in GI and how these challenges impact recruitment and research operations. • Maintain and deliver accurate, real-time analytics on our ASN sites. • Drive site recruitment in new and existing therapeutic areas and geographies. • Build solutions to establish and grow a pipeline of high potential sites that are starting in, or naïve to, clinical research. • Develop a holistic site engagement and support model.

🎯 Requirements

• 7-9 years of related experience in the clinical research industry (CRO, sponsor, SMO, or investigative site) & at minimum, an honour's Bachelors Degree (ideally; Life Sciences, Health Sciences, Nursing, Pharmacy, or a related discipline) • - Experience developing and managing relationships with investigative sites, principal investigators, and site personnel. • - Strong understanding of the clinical trial lifecycle, including site feasibility, study startup, patient recruitment, and ICH-GCP/regulatory requirements. • - Excellent relationship management, communication, and influencing skills, with the ability to engage investigators, site personnel, and cross-functional stakeholders. • - Experience using data and performance metrics to identify opportunities, strengthen site partnerships, and improve study delivery. • - Experience in gastroenterology or inflammatory diseases is an asset