# Clinical Trial Assistant 2

**Company**: IQVIA
**Location**: Netanya
**Experience**: entry
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Netanya-Israel/CTA2---Sponsor-Dedicated---Israel_R1562347?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_0acf3a67-e83

## Description

At IQVIA, our Clinical Functional Service Partnership (CFSP) model offers the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA.

You'll develop deep, specialist expertise on a dedicated program, with the flexibility to expand across sponsors and therapeutic areas as your career progresses - and the security of a long-term IQVIA career even as individual programs evolve.

Through our long-standing partnerships with the world's leading pharmaceutical and biotechnology companies, you'll contribute to clinical research programs that bring innovative treatments to patients worldwide, working across all phases of development and a broad range of therapeutic areas, within a culture that supports flexibility, continuous learning, and wellbeing.

As a Clinical Trial Assistant 2 within Clinical FSP, you'll gain hands-on exposure to real study operations, build foundational expertise alongside experienced CRAs and Project Managers, and develop a clear path toward future clinical research roles, all within a global organization dedicated to transforming healthcare through human science and data science.

**Key Responsibilities:**

- Maintain and update Trial Master Files (TMF) and study documentation.

- Support document preparation, filing, tracking, and archiving.

- Review study files for completeness and compliance.

- Coordinate clinical trial supplies and tracking records.

- Assist with CRF tracking, study queries, and data workflows.

- Act as a key contact for project communications and documentation.

- Provide guidance and mentorship to Clinical Trial Assistants, supporting onboarding, training, and knowledge sharing across the team.

- Serve as a subject matter expert for clinical trial processes and may lead CTA study teams and contribute to recruitment activities.

- Support departmental quality and process improvement initiatives

**What You'll Bring:**

- Passion for clinical research and healthcare

- Science degree preferred

- Hebrew and English Languages at advanced level

- Minimum 1 years of clinical trials support experience

- Proficiency in Microsoft Office (Word, Excel, PowerPoint)

- Strong organisation skills and attention to detail

- Ability to manage multiple priorities and meet deadlines

- Effective communication skills with the ability to work collaboratively across teams

## Skills

### Required
- Microsoft Office
- clinical trials support
- Hebrew
- English
- organisation skills
- communication skills

### Nice to have
- science degree

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Netanya-Israel/CTA2---Sponsor-Dedicated---Israel_R1562347?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)