CDA I

Overview

Clinical Data Associate I role performing entry-level data cleaning for clinical trials, in accordance with GCPs and SOPs/WPDs.

What you'll do

• Identify, resolve and update data discrepancies.
• Make changes to the data management database as required.
• Generate, track and resolve data clarifications and queries.
• May implement CRF design in an identified graphic design package.

What you'll need

• 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.
• 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 environment and independently as needed.
• Must demonstrate good judgment in making decisions.
• Understands project protocol and Data Validation Manual.

Details

• Work schedule: standard, Monday to Friday.
• Work is performed in an office or clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations.
• Potential occasional travel required.