# Senior Clinical Data Manager- Data Standards

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/South-Africa-Johannesburg/Senior--Clinical-Data-Manager--Data-Standards_JR161900?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_de6c227e-a34

## Description

As a Senior Manager, Clinical Data Management at ICON, you will be client dedicated, leading the development and implementation of clinical data standards processes that support high-quality data delivery across global clinical trials.

You will play a key role in driving data quality, standards development, data review, and continuous improvement initiatives while partnering with cross-functional stakeholders across the clinical development lifecycle.

**Key Responsibilities**

- Lead the development and operationalisation of clinical data standards processes and best practices.

- Drive initiatives related to data cleaning, data quality, edit checks, data listings, and standards library management.

- Partner closely with Clinical Trial Reporting (CTR), Clinical Trial Configuration (CTC), and Cross-Functional Data Review (CFDR) teams.

- Establish governance, workflows, and quality standards to support clinical trial delivery.

- Lead and mentor Associate Manager-level team members while fostering a culture of continuous improvement.

- Collaborate with cross-functional stakeholders to translate strategic objectives into operational execution.

- Identify risks, drive process improvements, and promote data quality across the clinical data lifecycle.

**You Will Have/Be:**

- Bachelor's degree in Life Sciences, Health Sciences, or a related discipline.

- Extensive Clinical Data Management experience within a CRO, biotechnology, or pharmaceutical environment.

- Strong experience in process development, project management, stakeholder engagement, and cross-functional collaboration.

- Proven ability to build and operationalise new processes and ways of working.

- Experience in data quality, standards development, data review, edit checks, data listings, or standards library management.

- Strong understanding of clinical trial processes, regulatory requirements, and ICH-GCP.

- Excellent communication, problem-solving, and leadership skills.

- An entrepreneurial mindset with the ability to thrive in a developing and evolving function.

**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
- Clinical Data Management
- data quality
- standards development
- data review
- edit checks
- data listings
- standards library management
- ICH-GCP
- Life Sciences
- Health Sciences

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