Global Site Id And Feasibility Analyst

Iqvia; Gauteng; On-site; ZAR 30 000 - 60 000; Full time

Job summary

An established industry player is seeking a Global Site ID and Feasibility Analyst to support the administration of clinical systems. In this role, you will collaborate with clinical study teams, conduct data analysis, and assist with feasibility launches. Your expertise will drive the selection of suitable sites for clinical studies, ensuring data accuracy and effective communication with stakeholders. Join a dynamic team where your contributions will shape the future of clinical research and enhance patient outcomes. If you are passionate about clinical trials and thrive in a collaborative environment, this opportunity is perfect for you.

Qualifications

• 3+ years of clinical trial experience or 2+ years in feasibility/recruitment.
• Knowledge of clinical research and drug development concepts.

Responsibilities

• Collaborate with clinical study teams to ensure data accuracy.
• Conduct research to identify potential sites meeting study criteria.

Skills

Clinical Trial Experience

Data Analysis

Project Management

Stakeholder Collaboration

Excel Proficiency

Education

B.S. in Scientific or Health-Related Field

Tools

CTMS

Trial Optimization Tools

Job description

Join to apply for the Global Site ID and Feasibility Analyst role at IQVIA

Job Summary

The Global Site Identification and Feasibility specialist supports the administration of clinical systems and tools used by Development Operations.

Works closely with Development Operations teams, study start-up, and CROs to provide key inputs, metrics, and outputs to support the selection of suitable sites for clinical studies.

Essential Functions

1. Collaborate with clinical study teams to ensure data accuracy in CTMS.
2. Support end users of clinical systems, evaluate and recommend on issue/enhancement requests under supervision.
3. Conduct research and data analysis to identify potential sites meeting study criteria.
4. Assist with feasibility launch, including system setup, questionnaire creation, and outreach.
5. Communicate effectively with study teams and stakeholders to support feasibility activities.
6. Track feasibility responses and report to stakeholders.
7. Troubleshoot issues in the feasibility process.
8. Stay updated on regulations and industry trends related to site feasibility.
9. Support enrollment forecasting and scenario discussions with stakeholders.

Minimum Requirements

• B.S. in a scientific or health-related field (or equivalent) with 3+ years of clinical trial experience and/or 2+ years in feasibility/recruitment.
• Experience with trial optimization vendors, tools, and methods.
• Knowledge of clinical research and drug development concepts.
• Experience collaborating with internal and external stakeholders.
• Ability to prioritize multiple projects within tight timelines.
• Administrative and project management skills in academic, CRO, or sponsor environments.
• Experience in multiple rare disease therapeutic areas.
• Data analysis and interpretation skills.
• Proficiency in Excel.