Job Summary:
We are seeking an experienced Clinical Trial Site Alliance Manager to lead the development and execution of strategic partnerships with clinical trial sites, investigators, and institutions. The successful candidate will be responsible for building and maintaining relationships, identifying new business opportunities, and driving revenue growth. This is a full-time, on-site role and will be based on strategic sites. The Site Alliance Manager will support the CRAs/PM team on site and their primary role will be to ensure compliance with research activities and deliverables with clinical trial sites and will be responsible for the Day-to-day tasks.
Key Accountabilities:
Supervise daily site operations and ensure compliance with protocol, SOPs and regulations.
Support CRAs and study team in site management activities, including issue resolution and escalation.
Coordinate with site and Xcene study team (including study vendors) and stakeholders to meet project goals.
Support site to address challenges and implement solutions to enhance efficiency.
Maintain clear documentation and reporting on site activities.
Key Responsibilities:
Site Relationship Management: Develop and maintain strong relationships with clinical trial sites, investigators, and institutions.
Partnership Development: Identify, develop, and maintain strategic partnerships with clinical trial sites, investigators, and institutions.
Business Development: Identify new business opportunities and develop strategies to pursue them.
Study Start-Up: Collaborate with cross-functional teams to ensure efficient study start-up, including site selection, contract negotiation, and budgeting.
Site Performance Management: Monitor and manage site performance, including enrollment, data quality, and compliance.
Issue Resolution: Resolve issues and concerns with clinical trial sites, investigators, and institutions.
Contract Management: Negotiate, manage, and enforce contracts with clinical trial sites, investigators, and institutions.
Compliance: Ensure compliance with regulatory requirements, including GCP, ICH, and FDA regulations.
Requirements:
Education:
Bachelor’s degree in Life Sciences, Nursing, or related field.
Experience:
Minimum 5 years of experience in clinical trials, including site management, study coordination, or related roles.
Skills:
Strong communication, negotiation, and interpersonal skills.
Proven ability to build and maintain relationships with clinical trial sites, investigators, and institutions.
Strong knowledge of clinical trials, including GCP, ICH, and FDA regulations.
Ability to work in a fast-paced environment and prioritize multiple projects.
Submit your CV to humanresources@xceneresearch.com
Apply via :
humanresources@xceneresearch.com