# Clinical Research Associate (CRA)

**Company**: Syneos Health
**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/CTM---Future-Roles--UK-_25106984?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_38f42fcf-515

## Description

Syneos Health is seeking a Clinical Research Associate (CRA) to join their team.

The CRA 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 process of obtaining informed consent and document confidentiality of subjects/patients

- Assess factors affecting subject/patient's safety and clinical data integrity

- Conduct Source Document Review and verify clinical data entered in case report forms

- Apply query resolution techniques and provide guidance to site staff

- Utilize available hardware and software to support clinical project data review and capture

- Perform investigational product inventory, reconciliation, and reviews storage and security

- Routinely review Investigator Site File and reconcile contents with Trial Master File

- Document activities via confirmation letters, follow-up letters, trip reports, and communication logs

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

- Enter data into tracking systems to track observations and action items

- Understand project scope, budgets, and timelines, and manage site-level activities

- Act as primary liaison with project site personnel and ensure training and compliance

- Prepare for and attend Investigator Meetings and sponsor face-to-face meetings

- Provide guidance on audit readiness standards and support preparation for audits

For Real World Late Phase, the CRA I will use the business card title of Site Management Associate I. Additional responsibilities include:

- Site support throughout the study lifecycle

- Knowledge of local requirements for real-world late-phase study designs

- Chart Abstraction activities and data collection

- Collaboration with Sponsor affiliates, medical science liaisons, and local country staff

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

- Good computer skills and ability to adapt to new technologies

- Excellent communication, presentation, and interpersonal skills

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

## Skills

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

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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/CTM---Future-Roles--UK-_25106984?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)