# Clinical Research Associate

**Company**: Syneos Health
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: $base salary range represents the anticipated low and high of the Syneos Health range for this position
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Research-Associate---Full-Service_25109785?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7772b9c5-209

## Description

Syneos Health is seeking a Clinical Research Associate. As a Clinical Research Associate, you will perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.

Responsibilities:

- Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits

- Evaluate overall performance of site and site staff and provide recommendations regarding site-specific actions

- Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient

- Assess factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site

- Conduct Source Document Review of appropriate site source documents and medical records

- Verify required clinical data entered in the case report form (CRF) is accurate and complete

- Apply query resolution techniques remotely and on site, and provide guidance to site staff as necessary

- Utilize available hardware and software to support the effective conduct of the clinical study data review and capture

- Verify site compliance with electronic data capture requirements

- May perform investigational product (IP) inventory, reconciliation, and reviews storage and security

- Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness, and completeness

- Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents

- Supports subject/patient recruitment, retention, and awareness strategies

- Enters data into tracking systems as required to track all observations, ongoing status, and assigned action items to resolution

Qualifications:

- Bachelor's degree or RN in a related field or equivalent combination of education, training, and experience

- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements

- Must demonstrate good computer skills and be able to embrace new technologies

- Excellent communication, presentation, and interpersonal skills

- Ability to manage required travel of up to 75% on a regular basis

Benefits:

- Company car or car allowance

- Health benefits to include Medical, Dental, and Vision

- Company match 401k

- Eligibility to participate in Employee Stock Purchase Plan

- Eligibility to earn commissions/bonus based on company and individual performance

- Flexible paid time off (PTO) and sick time

## Skills

### Required
- Good Clinical Practice
- ICH Guidelines
- regulatory requirements
- computer skills
- communication skills
- interpersonal skills

---

Source: [Apply at syneoshealth.wd12.myworkdayjobs.com](https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/USA-NC-Remote/Clinical-Research-Associate---Full-Service_25109785?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)