CDA I Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Clinical Data Associate I – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to perform entry-level aspects of the data cleaning process with a high level of accuracy and in accordance with GCPs and SOPs/WPDs to assess the safety and efficacy of investigational products and/or medical devices. What You’ll Do:

- Identifies, resolves, and updates data discrepancies. Makes changes to the data management database as required.
- Generates, tracks and resolves data clarifications and queries.
- May implement CRF design in identified graphic design package.

Education and Experience Requirements

- High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification • Technical positions may require a certificate • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years). In some cases an equivalency, consisting of a combination of appropriate education,



training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities:
- Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations • Strong attention to detail and skill with numbers • Ability to use interactive computer programs • Good written and verbal communication skills and a solid command of English language and grammar • Good analytical /problem-solving skills • Ability to work productively with direct supervision • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Proven flexibility and adaptability • Ability to work in a team environment and independently as needed • Must demonstrate good judgment in making decisions • Understands project protocol and Data Validation Manual Working Conditions and Environment:
- Work is performed in an office or clinical environment with exposure to electrical office equipment.
- Occasional drives to site locations.

Potential

Occasional travel required. •

📌 Clinical Data Associate (Bengaluru)
🏢 Thermo Fisher Scientific India
📍 Bengaluru