# Clinical Trial Subject Matter Expert (CT SME)

**Company**: ICON
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/South-Africa-Johannesburg/Clinical-Trial-SME_JR157188?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_089f79b4-e25

## Description

ICON is seeking a Clinical Trial Subject Matter Expert (CT SME) to join their team. As a CT SME, you will use your clinical research experience to assist colleagues in producing accurate and engaging components for stakeholders. You will work independently or with the team to create high-quality digital solutions that meet sponsor needs and expectations.

Responsibilities:

- Use clinical research experience to assist colleagues in producing accurate and engaging components

- Work independently or with the team to create high-quality digital solutions

- Advise and support the production team on clinical trial-related matters

- Ensure technical accuracy of products/solutions at each stage of development

- Conduct comprehensive reviews of study documentation

- Attend sponsor meetings and assist the Project Manager as required

- Communicate/escalate protocol-related queries to the Project Manager/In Team Lead

- Maintain a working knowledge of ICH/GCP Guidelines and relevant regulations

- Assume additional responsibilities as directed by the CTSME Supervisor

- Identify operational efficiencies and process improvements

- Assist in training and mentoring less experienced CT SMEs

- Maintain a high personal level of knowledge concerning current regulation and changes within the clinical research industry

Profile:

- B.Sc. (Hons) in life science or equivalent

- Minimum 2-3 years' experience as a CRA/site coordinator/study nurse within the clinical research industry

- Experience across different trial phases and therapeutic areas

- Excellent practical knowledge and understanding of clinical trials and experience with different clinical trial systems/vendors

- Excellent analytical skills and attention to detail

- Ability to work independently and as part of a project team

- Ability to produce accurate work within tight deadlines

- Knowledge of ICH GCP guidelines and experience in reviewing study-related documentation

- Excellent written and verbal communication in English

Rewards & Benefits:

- Competitive base salary and performance-related incentives

- Health and wellbeing programmes, including medical, dental, and vision coverage

- 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
- ICH GCP guidelines
- clinical research
- life science
- analytical skills
- communication skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/South-Africa-Johannesburg/Clinical-Trial-SME_JR157188?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)