Site Navigator I
Location: remote
We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to grow their career in clinical research within a global CRO environment.
Key Responsibilities
- Perform site identification feasibility and startup activities including site outreach feasibility questionnaires and confidentiality agreements
- Coordinate and track essential regulatory documents to ensure timely and compliant site activation
- Act as a primary point of contact for investigative sites during the startup and possibly the maintenance phase
- Perform ethics committee and regulatory authority submissions renewals and prepare the relevant regulatory documentation in collaboration with internal teams
- Perform site contract and budget negotiations under guidance
- Perform remote Pre-Study Visits
- Support Site Initiation Visit (SIV) preparation including coordination of documents systems access and study supplies
- Perform remote/inhouse CRA activities such as document review CRF review data validation and remote monitoring tasks (after required training)
- Maintain accurate documentation in study systems and ensure the TMF is inspectionready
- Collaborate closely with CRAs project teams and study stakeholders to support study milestones
Qualifications
- University degree (life sciences preferred)
- Minimum 1 year experience in Clinical Operations or Start-Up
- Knowledge of ICH/GCP and clinical trial processes
- Strong organizational skills attention to detail effective communication and willingness to learn
- Ability to manage multiple tasks in a structured and proactive way
Learn more about our EEO & Accommodations request here.
Site Navigator ILocation: remoteWe are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to grow their career in clin...
Site Navigator I
Location: remote
We are looking for a clinical operations professional to join our team as Site Navigator I managing clinical trial startup activities with additional inhouse CRA responsibilities. This is an excellent comprehensive role for someone looking to grow their career in clinical research within a global CRO environment.
Key Responsibilities
- Perform site identification feasibility and startup activities including site outreach feasibility questionnaires and confidentiality agreements
- Coordinate and track essential regulatory documents to ensure timely and compliant site activation
- Act as a primary point of contact for investigative sites during the startup and possibly the maintenance phase
- Perform ethics committee and regulatory authority submissions renewals and prepare the relevant regulatory documentation in collaboration with internal teams
- Perform site contract and budget negotiations under guidance
- Perform remote Pre-Study Visits
- Support Site Initiation Visit (SIV) preparation including coordination of documents systems access and study supplies
- Perform remote/inhouse CRA activities such as document review CRF review data validation and remote monitoring tasks (after required training)
- Maintain accurate documentation in study systems and ensure the TMF is inspectionready
- Collaborate closely with CRAs project teams and study stakeholders to support study milestones
Qualifications
- University degree (life sciences preferred)
- Minimum 1 year experience in Clinical Operations or Start-Up
- Knowledge of ICH/GCP and clinical trial processes
- Strong organizational skills attention to detail effective communication and willingness to learn
- Ability to manage multiple tasks in a structured and proactive way
Learn more about our EEO & Accommodations request here.
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