# Single Sponsor Clinical Project Manager II (Virology)

**Company**: Syneos Health
**Location**: Uxbridge
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GBR-London-Hybrid/Single-Sponsor-Clinical-Project-Manager-II--Virology----3-days-a-week-in-Uxbridge_25109273?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_686a0c12-5b1

## Description

Syneos Health is seeking a Single Sponsor Clinical Project Manager II (Virology) to join their team.

The successful candidate will be responsible for managing clinical projects, specifically in the virology team, with 1-2 days in Uxbridge and office move to Central London in May 2026.

**Job Responsibilities:**

- Plan, direct, create, and communicate clinical study timelines to ensure deliverables are produced on schedule

- Gather input from cross-functional teams to create comprehensive plans for clinical studies

- Ensure consistency of clinical study processes across clinical trials, adhering to standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations

- Oversee and resolve operational aspects of clinical trials in conjunction with project teams

- Select sites and vendors, prepare clinical trial budgets, and ensure studies are conducted within clinical trial protocols

- Monitor progress and follow up with team members and line managers when issues develop

- Implement and prepare the clinical development strategy as outlined by the clinical teams

- Develop trial recruitment strategies to ensure successful participant enrollment

**Qualifications:**

- Bachelor's degree in a related field (e.g., Clinical Research, Life Sciences, Healthcare Management)

- Minimum of 5 years of experience in clinical project management or a related role

- Proven track record of successfully managing clinical trials and ensuring adherence to SOP, GCP, and country regulations

**Certifications:**

- Certification in Clinical Research (e.g., CCRP, CCRA) is preferred

- Project Management Professional (PMP) certification is a plus

**Necessary Skills:**

- Strong organizational and planning skills to create and manage clinical study timelines

- Excellent communication skills to gather input from cross-functional teams and communicate plans effectively

- Ability to oversee and resolve operational aspects of clinical trials

- Knowledge of SOP, GCP, and country regulations to ensure consistency across clinical studies

- Experience in site and vendor selection, budget preparation, and monitoring progress

- Ability to implement and prepare clinical development strategies

- Strong problem-solving skills to address issues that arise during clinical trials

## Skills

### Required
- Clinical Research
- Life Sciences
- Healthcare Management
- Project Management
- Good Clinical Practice (GCP)
- Standard Operating Procedures (SOP)

### Nice to have
- CCRP
- CCRA
- PMP

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GBR-London-Hybrid/Single-Sponsor-Clinical-Project-Manager-II--Virology----3-days-a-week-in-Uxbridge_25109273?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)