Smart Workplace Consulting Director
Saegus51 – 200 Employees
Consulting
Lead Saegus’s Smart Workplace business unit, overseeing its strategy, profit and loss, enterprise accounts, and workplace transformation programs.
Open
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
Senior Clinical Research Associate – South Africa (Remote)
Senior Clinical Research Associate overseeing site monitoring and trial execution for ICON’s sponsor-dedicated research programs. The role focuses on protocol compliance, site performance, data quality, and regulatory standards.
Description
- Support sponsor-dedicated research programs using ICON’s global clinical expertise
- Manage clinical trial activities in line with protocols, regulations, and industry standards
- Lead technically complex monitoring work with a focus on quality and ongoing improvement
- Evaluate site adherence to study protocols, regulatory requirements, and Good Clinical Practice standards
- Conduct site visits to review performance, address issues, and help deliver trials successfully
- Partner with cross-functional teams to support timely, accurate data collection and reporting
- Train and advise site staff and fellow Clinical Research Associates
- Develop relationships with site personnel and stakeholders to support efficient trial operations
Requirements
- Bachelor’s degree in a relevant scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience with a strong grasp of clinical trial processes and regulatory requirements
- Demonstrated ability to coordinate multiple sites and projects while applying strong organization and problem-solving skills
- Advanced knowledge of monitoring methods, data integrity, and site management, including relevant clinical trial software and tools
- Strong communication, interpersonal, and stakeholder management abilities, with the capacity to influence compliance in a complex environment
- Availability to travel as needed, approximately 60% of the time
- Legal authorization to work in the country where the role is located
Benefits
- Base salary with performance-related incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Structured training and career development opportunities
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