Data Process Associate

About the Role

Step into the critical role of a Data Process Associate and contribute to the success of clinical trials by ensuring accurate and compliant data management. This role offers you the chance to develop key skills, work alongside experienced professionals, and build a strong foundation for your future in clinical research. If you're detail-focused and driven to support meaningful healthcare advancements, this is your opportunity to grow and make a difference.

Key Responsibilities

• Accurately enter and verify clinical data from Case Report Forms (CRFs) into study databases in accordance with established guidelines.
• Perform quality control checks to ensure data accuracy, integrity, and compliance with regulatory requirements.
• Assist with database testing, documentation preparation, and clinical data processing across multiple projects.
• Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation.
• Collaborate with project managers and cross-functional teams to ensure timely completion of data management activities.
• Identify process improvement opportunities and contribute to maintaining high-quality standards.
• Perform medical coding activities and other assigned tasks to support successful study completion.

What You Will Gain

• Gain hands-on experience in clinical data management within a regulated and fast-paced environment.
• Develop an in-depth understanding of industry standards, including ICH guidelines, Good Clinical Practice (GCP), and data handling regulations.
• Gain exposure to project management and collaboration with global cross-functional clinical research teams.
• Strengthen analytical, communication, and technical skills using industry-leading tools and systems.
• Build a strong foundation for career growth in clinical research and data management.
• Contribute to clinical studies that help advance healthcare and improve patient outcomes.

Requirements & Tech Stack

• Master’s degree in Life Sciences or a related field.
• Basic knowledge of Clinical Data Management.
• Strong analytical skills with excellent attention to detail.
• Good verbal and written communication skills.
• Basic knowledge of ICH Guidelines and Good Clinical Practice (GCP), including regulatory requirements related to clinical development programs, data handling, and data processing.
• Proficiency in PC applications, including Microsoft Excel and Microsoft Word.
• Ability to manage multiple competing priorities in a dynamic and fast-changing environment.
• Ability to work effectively within teams, inspire collaboration, and motivate colleagues to achieve project goals.
• Strong organizational and problem-solving skills.
• Ability to maintain accuracy and quality while working under deadlines.

Benefits

• Competitive salary
• Six Month Intensive Training Plan
• Flexible working hours
• Holidays (Annual Leave, Sick Leave, Casual Leave and Bank holidays)
• Medical Insurance for self and immediate family
• Gratuity
• Accidental Coverage
• Variety of different learning development opportunities (mentoring, coaching, e-learning, job shadowing)