# Senior Clinical Research Associate - Surgical Device - Central Region

**Company**: ICON Strategic Solutions
**Experience**: senior
**Job type**: full-time
**Salary**: $110,520.00-$138,150.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Texas/Senior-Clinical-Research-Associate---Medical-Device_JR162368?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_51488aa4-333

## Description

As a Senior Clinical Research Associate - Surgical Device - Central Region at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:

- 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.

You will have a strong foundation in clinical trial monitoring, with the experience of working independently and guiding others. Required qualifications and experience:

- A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing, or Biological Science.

- 3-5 years of CRA monitoring experience in CRO/pharma environments.

- Strong preference for at least 1 year of medical device monitoring experience; however, complex pharma monitoring experience will be considered.

- In-depth knowledge of FDA regulations and ICH/GCP guidelines.

- Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.

- Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.

- Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.

- Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.

- Ability to work independently and manage multiple priorities in a dynamic environment.

- A well-executed plan for communication with the study teams and sites.

- Well-versed in clinical trial management; rigorous, detail-oriented, and precise in reports.

- Willingness to travel as required (approximately 60%).

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- 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)
- FDA regulations
- ICH guidelines
- clinical trial management
- problem-solving
- interpersonal skills
- verbal and written communication

### Nice to have
- medical device monitoring experience

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Texas/Senior-Clinical-Research-Associate---Medical-Device_JR162368?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)