Senior Site Navigator
Job Code: 700344 Job Level: P2 Individual Contributor Function: Clinical Operations Work Model: Remote / Office-based with travel as needed
About the Role
As a Senior Site Navigator youll act as a local country or regional expert in study start-up leading site-level activities with minimal oversight. Youll be a trusted partner to sites and internal teams proactively identifying risks mentoring junior colleagues and ensuring studies move forward efficiently and compliantly. 700344 - PDF
What Youll Be Doing
Lead and oversee site start-up and activation activities across assigned studies
Act as a knowledge resource and mentor for junior Site Navigators
Manage site outreach feasibility pre-study visits and regulatory documentation
Serve as the primary site contact ensuring high-quality delivery aligned with study scope and budgets
Support IRB/IEC and regulatory authority submissions renewals and compliance activities
Lead contract and budget negotiations with investigative sites
Ensure TMF accuracy inspection readiness and system compliance
Collaborate with CRAs study leads vendors and regulatory teams to support SIVs and ongoing study needs
Anticipate and mitigate risks that may impact timelines or site performance
Participate in remote and on-site activities as required to support study success 700344 - PDF
What Were Looking For
Education & Experience
University/College degree (life sciences preferred) or equivalent clinical research experience
3 years of experience in clinical research start-up or regulatory processes
Strong hands-on knowledge of ICH/GCP IRB/IEC and regulatory frameworks
Skills & Competencies
Proven ability to manage complex site portfolios independently
Strong negotiation skills (contracts and budgets)
Excellent stakeholder communication and leadership presence
Ability to mentor guide and influence others
Fluency in English and the local official language (written and spoken) 700344 - PDF
Why This Role
This role is ideal for experienced professionals ready to lead mentor and shape site start-up strategy while continuing to grow within a high-impact clinical operations environment.
Learn more about our EEO & Accommodations request here.
Required Experience:
Senior IC
Senior Site NavigatorJob Code: 700344 Job Level: P2 Individual Contributor Function: Clinical Operations Work Model: Remote / Office-based with travel as neededAbout the RoleAs a Senior Site Navigator youll act as a local country or regional expert in study start-up leading site-level activities wi...
Senior Site Navigator
Job Code: 700344 Job Level: P2 Individual Contributor Function: Clinical Operations Work Model: Remote / Office-based with travel as needed
About the Role
As a Senior Site Navigator youll act as a local country or regional expert in study start-up leading site-level activities with minimal oversight. Youll be a trusted partner to sites and internal teams proactively identifying risks mentoring junior colleagues and ensuring studies move forward efficiently and compliantly. 700344 - PDF
What Youll Be Doing
Lead and oversee site start-up and activation activities across assigned studies
Act as a knowledge resource and mentor for junior Site Navigators
Manage site outreach feasibility pre-study visits and regulatory documentation
Serve as the primary site contact ensuring high-quality delivery aligned with study scope and budgets
Support IRB/IEC and regulatory authority submissions renewals and compliance activities
Lead contract and budget negotiations with investigative sites
Ensure TMF accuracy inspection readiness and system compliance
Collaborate with CRAs study leads vendors and regulatory teams to support SIVs and ongoing study needs
Anticipate and mitigate risks that may impact timelines or site performance
Participate in remote and on-site activities as required to support study success 700344 - PDF
What Were Looking For
Education & Experience
University/College degree (life sciences preferred) or equivalent clinical research experience
3 years of experience in clinical research start-up or regulatory processes
Strong hands-on knowledge of ICH/GCP IRB/IEC and regulatory frameworks
Skills & Competencies
Proven ability to manage complex site portfolios independently
Strong negotiation skills (contracts and budgets)
Excellent stakeholder communication and leadership presence
Ability to mentor guide and influence others
Fluency in English and the local official language (written and spoken) 700344 - PDF
Why This Role
This role is ideal for experienced professionals ready to lead mentor and shape site start-up strategy while continuing to grow within a high-impact clinical operations environment.
Learn more about our EEO & Accommodations request here.
Required Experience:
Senior IC
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