# Sr CRA I/II - Sweden, Sponsor-dedicated (Pipeline)

**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/SWE-Remote/Sr-CRA-I-II---Sweden--Sponsor-dedicated--Pipeline-_25101241?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_8a652544-c31

## Description

Syneos Health is seeking a Sr CRA I/II - Sweden, Sponsor-dedicated (Pipeline). As a Sr CRA, you will play a critical role in ensuring the quality and compliance of clinical trials.

**Job Responsibilities**

- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices

- 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 compliance
- data analysis
- communication

### Nice to have
- Certified Clinical Research Professional
- clinical trial management systems

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Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/SWE-Remote/Sr-CRA-I-II---Sweden--Sponsor-dedicated--Pipeline-_25101241?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)