Uat Test Analyst/Clinical Data Analyst I - South Africa, Remote - Fsp

Findojobs South Africa; South Africa; Remote; ZAR 200,000 - 300,000; Full time

Job summary

A leading clinical research organization is seeking UAT Test Analysts / Clinical Data Analysts for a fully remote position in South Africa. The role involves data validation, managing clinical database setups, and ensuring compliance with quality standards in clinical studies. Candidates must have strong problem-solving skills and a background in clinical data management. This opportunity offers flexibility and a chance to contribute to patient well-being.

Qualifications

• Strong problem-solving skills and logical reasoning.
• Effective time management and prioritization skills.
• Fluency in English, both written and oral.

Responsibilities

• Perform UAT testing on clinical database setups.
• Lead data cleaning and review activities.
• Support data processing from database setup to lock.

Skills

Problem-solving

Time management

Team collaboration

Interpersonal communication

Analytical skills

Adaptability

Education

Bachelor’s degree or medical qualifications

Tools

Microsoft Office

Clinical Data Management Systems

Job description

When our values align, there's no limit to what we can achieve.

Parexel is currently recruiting for UAT Test Analysts / Clinical Data Analysts in South Africa.

In this role, successful individuals will work under the guidance and supervision of their Line Manager and/or Subject Matter Experts to perform UAT testing and some clinical data cleaning activities on assigned projects. Responsibilities may also include support for data processing activities, Data Management documents, and data cleaning matrices such as Data Validation specifications, CRF Completion Guidelines, Protocol Deviation Specifications, Mock Shells for Offline listing, etc.

This is a fully remote, home-based position.

Key Accountabilities :

• Data Validation (Cleaning): Responsible for leading data cleaning and review activities (Co-Primary CDA / Primary CDA), including query management and manual/SAS listing reviews.
• Support data processing activities from database setup to database lock, e.g., external vendor data reconciliation.
• Data Management Documents / Plans (Trial Master File): Perform and support the setup of DM documents, ensuring proper documentation as per SOPs, ICH / GCP Guidelines.
• Study Start-Up Activities and User Acceptance Testing (UAT):
Lead or perform UAT on clinical database setups and review protocols and EDC Entry Screens if required.
• Data Tracking and Entry:
Track and review CRFs and support data entry as needed.
• Project Quality Management & Compliance:
Ensure compliance with SOPs, ICH / GCP Guidelines, and support QC activities on databases and patient data.

What we are looking for in this role

We seek professionals with determination and courage to prioritize patient well-being, working with heart.

• Strong problem-solving skills and logical reasoning.
• Commitment to first-time quality with a methodical, analytical, and accurate approach.
• Effective time management and prioritization skills.
• Ability to work collaboratively within a team.
• Excellent interpersonal, oral, and written communication skills.
• Quick learning ability and knowledge sharing approach.
• Flexible attitude towards work assignments and adaptability to changing environments.
• Fluency in English, both written and oral.

Knowledge and Experience :

• Technical aptitude with experience in Microsoft Office.
• Understanding of data management processes and validation flow.
• Knowledge of ICH-GCP Guidelines, local regulations, and study procedures.
• Familiarity with Clinical Data Management Systems (e.g., InForm, Rave, Veeva, DataLabs, ClinBase).
• Experience in the clinical research industry.
• Basic knowledge of medical terminology and coding dictionaries (e.g., MedDRA, WHODRUG).
• Understanding of Data Management operational processes during all study phases.
• Knowledge of database setup activities, including configuration specifications and data validation setup.

Education :

Bachelor’s degree, medical qualifications, or relevant industry experience.

Who are Parexel

Parexel supports clinical studies across various therapeutic areas with longstanding partnerships. We have supported trials for many top-selling drugs and enable niche developments critical to patient well-being.