Site Network Manager; North America

Positions available: 1

Logistics: US-based coverage (some Canada), travel around 20% expected. Position is open to applicants based in the contiguous United States or Canada, and the successful candidate will need to be able to reasonably travel to their nearest airport.

Closing date:
July 24th, 2026

• 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) to expand the ASN
• 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
• Oversee the development and maintenance of an Investigator portal to enhance communication and onboarding of clinical sites to the ASN and clinical studies
• Support novel strategies for patient identification and engagement in partnership with ASN sites

• Build stakeholder engagement and collaboration through the adoption of change management methodologies and a strong focus on building key relationships
• Develop processes and workflows to support a scalable and growing ASN platform
• Drive and support (cross) departmental improvement initiatives to ensure company end to end processes and technologies are efficient and effective, work seamlessly together and deliver improved customer value
• Present and/or participate in specialized conferences/meetings to increase knowledge as needed
• Support contract negotiations as required

• 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