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Job Description & How to Apply Below
Overview
The Alimentiv Site Network Manager will be responsible for driving and delivering on the Alimentiv Site Network (ASN) Strategy, including project management, process optimization, and growth of the ASN globally.
Responsibilities- Manage identification, outreach, recruitment, and onboarding of high‑quality sites into the North America ASN.
- Develop strong relationships with high‑priority sites & partners through virtual or face‑to‑face meetings and conference attendance 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 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 new 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 adoption of change‑management methodologies.
- 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.
- Present and/or participate in specialized conferences/meetings to increase knowledge.
- Support contract negotiations as required.
- 7‑9 years of related experience in the clinical research industry (CRO, sponsor, SMO, or investigative site) and at minimum an honor’s bachelor’s degree (Life Sciences, Health Sciences, Nursing, Pharmacy or 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.
US‑based coverage (some Canada). Travel around 20% expected. Applicants must be based in the contiguous United States or Canada and be able to travel to nearest airport.
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