Senior Site Navigator
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 179d ago
The date the source published, not the day we noticed it (2026-05-11). Last seen at its source 1h ago.
We have tracked this listing since 22 Sep 2026 (44 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.
Is it remote?
Remote Brazil
That is the location the employer filed this posting under. Quoted as written — we do not re-word the source's own location.
Who may apply?
Brazil
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
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Workday employer's own board first seen 44d ago · last seen 1h ago
The listing
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, you’ll act as a local country or regional expert in study start-up, leading site-level activities with minimal oversight. You’ll be a trusted partner to sites and internal teams, proactively identifying risks, mentoring junior colleagues, and ensuring studies move forward efficiently and compliantly. [700344 - S...Navigator | PDF]
What You’ll Be Doing
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Lead and oversee site start-up and activation activities across assigned studies
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Act as a knowledge resource and mentor for junior Site Navigators
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Manage site outreach, feasibility, pre-study visits, and regulatory documentation
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Serve as the primary site contact, ensuring high-quality delivery aligned with study scope and budgets
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Support IRB/IEC and regulatory authority submissions, renewals, and compliance activities
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Lead contract and budget negotiations with investigative sites
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Ensure TMF accuracy, inspection readiness, and system compliance
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Collaborate with CRAs, study leads, vendors, and regulatory teams to support SIVs and ongoing study needs
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Anticipate and mitigate risks that may impact timelines or site performance
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Participate in remote and on-site activities as required to support study success [700344 - S...Navigator | PDF]
What We’re Looking For
Education & Experience
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University/College degree (life sciences preferred) or equivalent clinical research experience
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3+ years of experience in clinical research, start-up, or regulatory processes
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Strong hands-on knowledge of ICH/GCP, IRB/IEC, and regulatory frameworks
Skills & Competencies
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Proven ability to manage complex site portfolios independently
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Strong negotiation skills (contracts and budgets)
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Excellent stakeholder communication and leadership presence
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Ability to mentor, guide, and influence others
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Fluency in English and the local official language (written and spoken) [700344 - S...Navigator | 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.