CDA II Veeva

Work Schedule

Environmental Conditions

Job Description

Join Us as a Clinical Data Assoc II Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.

As part of our expert team youll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Assoc II you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs) to assess the safety and efficacy of investigational products and/or medical devices.

What Youll 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 identified graphic design package.
Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports.
Produce project-specific status reports for CDM management and for clients on a regular basis.
Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews.

Education and Experience Requirements:

• Life Science Graduation in Preferred
• Should have 4 Yers of experience in Clinical Data Manager role
• Should have experience in Veeva EDC

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 and ability to use interactive computer programs
Good written and verbal communication skills and a strong command of English language and grammar
Good organizational and analytical/problem-solving skills
Ability to work productively with moderate supervision
Ability to maintain a high degree of confidentiality with clinical data and clients proprietary data
Strong customer focus and excellent interpersonal skills.
Proven flexibility adaptability and ability to work in a team environment or independently as needed
Must demonstrate good judgment in making decisions
Knowledge of medical/clinical trial terminology
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.

Why Join Us

When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthroughs.