Clinical Data Associate II

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 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our expert team, you’ll 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 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 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:
  • 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 6 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 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 client's 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. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
  
  Apply today to help us deliver tomorrow’s breakthroughs.