# Biotech Site Monitor

**Company**: IQVIA
**Location**: Reading, Berkshire
**Experience**: entry
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/CRA-II----IQVIA-Biotech_R1576396?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/biotech-site-monitor-e41aa7bb-f41/

## Description

Join IQVIA Biotech, where innovation meets impact. You'll be at the forefront of groundbreaking therapies and novel diseases, often before they reach the broader scientific community.

**Responsibilities**

- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

- Work with sites to adapt, drive and track subject recruitment plans to enhance predictability.

- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites.

- Evaluate the quality and integrity of study site practices and escalate quality issues as needed.

- Manage study progress by tracking regulatory submissions, recruitment, case report form completion and data query resolution.

- Ensure site documents are available for filing in the Trial Master File (TMF) and verify Investigator's Site File (ISF) maintenance.

- Create and maintain documentation regarding site management, monitoring visit findings and action plans.

- Collaborate with study team members for project execution support.

**Qualifications**

- Minimum 1-2 years of on-site monitoring experience.

- Experience monitoring Oncology studies required.

- Bachelor's Degree in a scientific discipline or healthcare preferred.

- Basic knowledge of and skill in applying clinical research regulatory requirements (GCP and ICH guidelines).

- Good written and verbal communication skills, including command of English.

**Additional Requirements**

- Full UK right to work required; no visa sponsorship available.

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## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- Oncology studies
- English

### Nice to have
- Bachelor's Degree in scientific discipline or healthcare

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Reading-Berkshire-United-Kingdom/CRA-II----IQVIA-Biotech_R1576396?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)