Are you passionate about clinical research and data management? Novotech, a leading global clinical Contract Research Organization (CRO), is hiring for the role of Clinical Data Associate I in India. This is an exciting opportunity to work in the dynamic field of clinical trials and contribute to groundbreaking pharmaceutical research.
In this article, we’ll explore the job description, responsibilities, qualifications, and career growth opportunities for a Clinical Data Associate in India. Whether you’re a recent graduate or an experienced professional, this role offers a chance to work with a globally recognized organization committed to excellence in clinical research.
What Does a Clinical Data Associate Do?
A Clinical Data Associate (CDA) plays a crucial role in ensuring the accuracy and integrity of clinical trial data. This position involves:
- Data entry and validation using Clinical Data Management (CDM) software.
- Assisting in data cleaning, reconciliation, and query resolution.
- Supporting database testing and edit checks to ensure data quality.
- Collaborating with Clinical Data Managers (CDMs) and project teams to meet study objectives.
- Contributing to regulatory compliance by adhering to ICH-GCP guidelines and SOPs.
This role is ideal for individuals with a strong attention to detail and a passion for contributing to the advancement of medical research.
Key Responsibilities of a Clinical Data Associate
As a Clinical Data Associate I at Novotech, your responsibilities will include:
- Data Entry and Validation: Accurately entering and validating clinical trial data.
- Query Management: Reviewing and resolving data queries with sponsors and monitoring staff.
- Database Testing: Assisting in testing databases and edit checks.
- Reporting: Creating reports, listings, and other outputs as required.
- Project Support: Participating in project meetings and providing administrative support to CDMs.
- Compliance: Ensuring adherence to ICH-GCP, ISO 27001, and ISO 9001 standards.
Qualifications and Experience Required
To be eligible for the Clinical Data Associate I role, candidates should have:
- A graduate degree in a clinical or life sciences-related field.
- 6 months to 1 year of experience in the pharmaceutical or clinical research industry (preferred Not Mandatory).
- Knowledge of Clinical Data Management software and processes.
- Strong organizational and communication skills.
Novotech also values diversity and encourages applications from individuals who identify as LGBTIQ+, have disabilities, or have caring responsibilities.
Why Join Novotech?
Novotech is a global leader in clinical research, with over 3,700 clinical projects completed across Phase I to Phase IV trials. Here’s why you should consider joining their team:
- Inclusive Work Environment: Novotech is committed to gender equality and diversity.
- Professional Development: Opportunities for growth through training and industry conferences.
- Work-Life Balance: Flexible working options, paid parental leave, and wellness programs.
- Global Impact: Contribute to cutting-edge research that improves patient outcomes worldwide.
