Analytical Monitor

Icon Strategic Solutions; Johannesburg; On-site; ZAR 400 000 - 600 000; Full time

Job summary

A healthcare solutions company is seeking a candidate for a Clinical Analyst position in Johannesburg. The role involves conducting analytical monitoring and proactive issue detection across clinical trials. Applicants should have a Bachelor's degree in Health Sciences or Data Sciences and approximately 2+ years of relevant experience in the Pharmaceutical or Biotech industries. Strong data analysis, organizational, and communication skills are essential. Competitive salary with diverse benefits focused on well-being and work-life balance is offered.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits including childcare vouchers

Qualifications

• Approximately 2+ years of experience within the Pharmaceutical, CRO, Biotech or related industry.
• Understanding of clinical trial processes and regulatory frameworks.
• Experience with technology platforms for data analysis.

Responsibilities

• Conduct analytical monitoring activities across assigned clinical trials.
• Perform regular site/subject-level reviews to support proactive issue detection.
• Collaborate with Site Managers and other partners for risk management.

Skills

Data analysis and interpretation

Organizational skills

Interpersonal communication

English communication

Education

Bachelor's degree in Health Sciences, Data Sciences or related field

Tools

Data collection and reporting systems

Job description

What You Will Be Doing

Conducting analytical monitoring activities across assigned clinical trials to identify early trends, data quality issues, and potential risks at the site and subject level.

Performing regular (fit-for-purpose) site / subject-level reviews to support proactive issue detection and prevent recurrence.

Accessing and analysing data from multiple systems, databases, and reporting tools to derive insights that support informed decision-making.

Collaborating closely with Site Managers, Central Monitoring, and other cross-functional partners to influence site prioritisation and guided risk management.

Facilitating clear and effective communication with stakeholders, following escalation pathways where appropriate.

Ensuring all activities are performed in accordance with regulatory guidelines, SOPs, and ICON quality standards.

Your Profile

 Bachelor's degree in Health Sciences, Data Sciences or related field, or equivalent relevant experience.

 Approximately 2+ years of experience within the Pharmaceutical, CRO, Biotech or related industry.

 Strong experience in data analysis and interpretation within a clinical research environment.

 Understanding of clinical trial processes and working knowledge of ICH-GCP and regulatory frameworks.

 Experience with technology platforms and systems used for data collection, analysis, and reporting.

 Strong organisational skills, with the ability to manage multiple priorities in a fast-paced environment.

 Excellent communication and interpersonal skills, with the ability to collaborate effectively across global cross-functional teams and .

 Excellent verbal and written communication skills in English.

What ICON Can Offer You

In addition to your competitive salary, ICON offers a range of additional benefits focused on well-being and a work‑life balance for you and your family.

Our success depends on the quality of our people.

That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80, independent specialised professionals who are there to support you and your family's well‑being.
• Life assurance
• Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values.

We're dedicated to providing an inclusive and accessible environment for all candidates.

ICON is committed to providing a workplace free of discrimination and harassment.

All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements?

We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.