# Single Sponsor Senior CRA - Oncology

**Company**: Syneos Health
**Location**: GBR-Remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GBR-Remote/Single-Sponsor-Senior-CRA---Oncology--UK-based--Must-have-UK-on-site-and-risk-based-monitoring-exp---req-AB52F16606_25113382?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_98752e64-9fe

## Description

We are seeking a Single Sponsor Senior CRA - Oncology to join our team in the UK. As a Senior CRA, you will conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.

Responsibilities:

- Conduct on-site and remote monitoring of clinical research studies

- Develop and implement tools, procedures, and processes to ensure quality monitoring

- Contribute to the design, implementation, and delivery of processes, programs, and policies

- Manage and direct the work of lower-level professionals or manage processes and programs

- Ensure accurate and timely documentation and reporting of clinical trial data

- Collaborate with cross-functional teams to support clinical trial activities

- Identify and resolve issues related to clinical trial conduct and data integrity

- Provide training and mentorship to junior staff members

Qualifications:

- Bachelor's degree in a related field

- Minimum of 3-5 years of experience in clinical research or a related field

- In-depth knowledge of clinical trial processes and regulations

- Strong analytical and problem-solving skills

- Excellent communication and interpersonal skills

- Ability to work independently and as part of a team

Certifications:

- Certified Clinical Research Professional (CCRP) or equivalent certification preferred

Necessary Skills:

- Proficiency in clinical trial management systems and software

- Strong organizational and time management skills

- Attention to detail and accuracy

- Ability to manage multiple projects and priorities simultaneously

- Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

## Skills

### Required
- clinical trial management
- Good Clinical Practice
- regulatory requirements
- analytical skills
- communication skills

### Nice to have
- Certified Clinical Research Professional
- CCRP

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/GBR-Remote/Single-Sponsor-Senior-CRA---Oncology--UK-based--Must-have-UK-on-site-and-risk-based-monitoring-exp---req-AB52F16606_25113382?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)