Clin Data Assoc II

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

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 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 SOPsWPDs to assess the safety and efficacy of investigational products andor 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 projectspecific 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 andor 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 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

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 tomorrows breakthroughs