Data Process Associate
- Posted 2 days ago
- Be among the first 20 applicants
Job Description
Description
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.
What You Will Do
Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development
We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the carewyou want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.
Requirements
Education
Benefits
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.
What You Will Do
- 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.
- 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.
Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development
We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the carewyou want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.
Requirements
Education
- 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 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
- Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e-learning, job shadowing)
