Research Analyst

• Manage, deliver and/or perform full clinical site monitoring services for one or more projects, which may include multiple services, be complex in nature and/or run on a multinational scale.
• In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data/document management, monitoring project site budgets and regulatory filings that aligns with SOPs, study guidelines and GCP best practices.
• In the function of Lead CRA, will act as primary liaison between CRAs and project team and may be required to participate in the development of project plans, protocols, CRFs, communications or other monitoring forms, documents and tools.
• Represents the corporation by maintaining collaborative relationships with stakeholders.

Senior Clinical Research Associate

• Design, implement and manage research, evaluation and outcomes measurement projects for social, community and faith‑based programs, often leading project delivery while working collaboratively under senior direction
• Conduct qualitative and quantitative data analysis, identifying trends and patterns in complex datasets
• Working collaboratively within a diverse, multidisciplinary research team, engaging in mutual support and knowledge sharing by both offering and seeking guidance in qualitative and quantitative analysis, including the use of relevant analytical software
• Use statistical software (e.g. Excel, SPSS, R, SAS) to analyse large datasets within agreed timeframes
• Produce high-quality reports, literature reviews, dashboards, briefing papers and presentations tailored to internal and external stakeholders
• Review, develop and implement data collection systems, processes and procedures to optimise data quality and statistical efficiency
• Identify gaps and issues in data collection that hinder effective research and evaluation activities
• Actively explore and adopt new technologies, tools and methods to improve research efficiency and quality
• Conduct fieldwork activities such as surveys, interviews, focus groups and workshops in line with best practice
• Engage and support project stakeholders, including frontline services and partners
• Provide administrative and logistical support for research projects, including coordination of meetings, resources and travel
• Handle confidential and sensitive data ethically and with integrity.

• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects
• Conduct study initiation visits (SIVs)
• Ensure compliance with obtaining informed consent and reporting potential safety-related events

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Senior Clinical Research Associate

Research Analyst

Senior Clinical Research Associate