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 strong 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 workplace 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.

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📌 CDA I (India)
🏢 Thermo Fisher Scientific
📍 India