# Site Activation Manager

**Company**: Syneos Health
**Location**: CHE-Client
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHE-Client/Site-Activation-Manager_25113899?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_4f0f817c-03c

## Description

Syneos Health is seeking a Site Activation Manager to join their team in Luzern, Switzerland. As a Site Activation Manager, you will collaborate with major functional areas including Business Development, Alliance Management, and Project Management to ensure successful site activation and project deliverables.

Responsibilities:

- Collaborate with cross-functional teams to identify and evaluate fundamental issues pertaining to Site Start-Up, project regulatory pathway, and patient enrollment

- Ensure all project deliverables meet internal and customer expectations, providing accurate projections, reports, and updates

- Develop and maintain relationships with customers and ensure individual project targets and client needs are met

- Provide oversight of all project start-up deliverables, including life cycle maintenance regulatory activities and study maintenance

- Develop and manage integrated timelines and reports weekly progress, including plans to address potential timing risks/gaps

- Prepare and present overall SSU strategy and status at client meetings and communicate outcomes to project teams

- Review project SSU budget with functional leads, PM, and SSU Business Unit Controller against project milestones and budget

- Use professionally recognized tools for planning and management of scope, timeline, and resources

- Prepare core submission documents and core clinical trial application dossier for amendments

- Perform Regulatory Impact Assessment on core amendment submission documents and communicate risk mitigation to Sponsor/Project teams

- Assist in amendment updated development of master Subject Information Sheet (SIS) /Informed Consent Form (ICF)

- Oversee collation, quality review, and submission of country-specific applications

- Contribute to change initiatives across and within the SSU department

- Ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company SOP/Sponsor requirements

- Minimal travel may be required (up to 25%)

Syneos Health is committed to developing their people, building an inclusive culture, and delivering high-quality services to their customers.

## Skills

### Required
- regulatory affairs
- project management
- clinical trials
- site activation
- life sciences

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/CHE-Client/Site-Activation-Manager_25113899?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)