Catalyst Clinical Research, a global leader in clinical development solutions, is inviting applications for the position of Clinical Data Coordinator Trainee in Kochi, Kerala.
This is an exciting on-site, full-time opportunity for graduates eager to begin their career in clinical data management within the biopharmaceutical and biotechnology industries.
If you are detail-oriented, analytical, and passionate about advancing clinical studies through innovative data solutions, this role could be your gateway into the clinical research domain.
🧬 Key Responsibilities
As a Clinical Data Coordinator Trainee, you will play a pivotal role in ensuring the accuracy and integrity of clinical data for regulatory submissions and publications.
Your responsibilities include:
- Assisting in the development of edit specifications based on global medical standards and study protocols.
- Supporting data cleaning, coding, and validation activities using EDC and SAS systems.
- Reviewing manual data listings and submitting appropriate queries.
- Coordinating data reconciliation and quality control for patient records.
- Performing final patient reviews and assisting with database lock activities.
- Managing data transfers from external vendors (PK/PD, imaging, lab data).
- Contributing to SAE reconciliation and documentation in the data management plan.
🎓 Qualifications & Skills
Education:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related discipline (preferred).
- Freshers or candidates with up to one year of relevant experience are encouraged to apply.
Required Skills:
- Strong analytical and organizational abilities.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint).
- Excellent written and verbal communication skills.
- Ability to multitask and manage priorities in a dynamic environment.
- Collaborative mindset with strong interpersonal skills.
- Keen attention to detail and commitment to data quality and integrity.
🌟 Why Join Catalyst Clinical Research?
- Work with a global leader in oncology and multi-therapeutic CRO services.
- Gain exposure to cutting-edge clinical data management tools (EDC, SAS).
- Build a strong foundation in clinical operations and regulatory compliance.
- Learn from industry experts and be part of a supportive, innovation-driven culture.
- Opportunities for career progression in data management, biostatistics, and clinical research operations.
📝 How to Apply
