# Clinical Research Associate, CRA II, Senior CRA

**Company**: ICON
**Location**: Frankfurt, Germany
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Germany-Frankfurt/Clinical-Research-Associate-II---Senior-Clinical-Research-Associate-Large-Pharma-Biotech_JR155971?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_576b3275-753

## Description

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Senior/CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

**Responsibilities**

- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

**Your Profile**

- Master or Bachelor's degree in a scientific or healthcare-related field.

- Minimum of 2 years of experience as a Clinical Research Associate.

- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

- Strong organisational and communication skills, with attention to detail.

- Ability to work independently and collaboratively in a fast-paced environment.

- Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.

- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

- Excellent communication skills in German and English.

- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

- Ability to travel at least 60% of the time (international (DACH region) and domestic - fly and drive) and should possess a valid driver's license.

**Rewards & Benefits**

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

## Skills

### Required
- Good Clinical Practice (GCP)
- clinical trial management
- data integrity
- site management
- German
- English

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Germany-Frankfurt/Clinical-Research-Associate-II---Senior-Clinical-Research-Associate-Large-Pharma-Biotech_JR155971?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)