# Senior CRA in Oncology - Single Sponsor

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

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TUR-Istanbul/Senior-CRA-in-Oncology---Single-Sponsor---Based-in-Tukey_25112396?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_30cef860-e9f

## Description

We are seeking a Senior CRA in Oncology - Single Sponsor based in Turkey.

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

**Job Responsibilities**

- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms

- Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates

- Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials

- Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues

- Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans

- Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

**Qualifications:**

- Bachelor's degree in a related field or equivalent experience

- Minimum of 3-4 years of experience in clinical research monitoring

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

- Excellent communication and interpersonal skills

- Ability to work independently and manage multiple priorities

- Proficiency in using clinical trial management systems and other relevant software

**Certifications:**

- Certified Clinical Research Associate (CCRA) or equivalent certification preferred

**Necessary Skills:**

- Attention to detail and strong analytical skills

- Problem-solving abilities and critical thinking

- Ability to work effectively in a team environment

- Strong organizational and time management skills

- Proficiency in Microsoft Office Suite

## Skills

### Required
- Good Clinical Practice (GCP)
- clinical research monitoring
- clinical trial management systems
- Microsoft Office Suite

### Nice to have
- Certified Clinical Research Associate (CCRA)

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/TUR-Istanbul/Senior-CRA-in-Oncology---Single-Sponsor---Based-in-Tukey_25112396?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)