Data Process Associate

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 following established guidelines.
- Perform quality control checks to ensure data integrity and compliance with regulatory standards.
- Assist in database testing, documentation preparation, and processing of clinical data for 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 delivery of data management tasks.
- Identify opportunities to improve processes and contribute to maintaining high-quality standards.
- Perform medical coding activities and other assigned tasks to support study completion.

**What You Will Gain**:

- Hands-on experience in clinical data management within a regulated and fast-paced environment.
- In-depth understanding of industry standards, including ICH guidelines, GCP, and data handling regulations.
- Exposure to project management and teamwork across global, cross-functional clinical research teams.
- Development of strong analytical, communication, and technical skills using industry-leading tools and systems.
- A solid foundation for career growth in clinical research and data management disciplines.
- The opportunity to contribute to impactful clinical studies that advance healthcare and patient outcomes.
- Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs._
- 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 career you want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter._

**Requirements**:
**Education**:

- Qualified to Masters in life sciences background

**Skills, Knowledge, and Experience**:

- PC skills, including some knowledge of Excel and Word.
- Basic knowledge of Clinical Data Management.
- Analytical skills and attention to detail.
- Good communication skills (oral and written).
- Basic knowledge of ICH Guidelines and GCP, including regulatory requirements for the conduct of clinical development programs, especially related to data handling and processing.
- Ability to manage competing priorities in a changeable environment.
- Ability to inspire effective teamwork and motivate staff.

**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)