Senior Clinical Data Associate

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Data Associate 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 Senior Clinical Data Associate you will perform all aspects of the data cleaning process with minimal supervision in accordance with Good Clinical Practices (GCP) 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:
Supports the setup of study activities such as database design testing of data entry screens and Data Validation Manual (DVM) creation as required.
Reviews data listings for accuracy and consistency of data.
Acts as point person and subject matter expert for specialized study-specific processes.
Generates tracks and resolves data clarifications and queries and makes changes to the clinical database as required.
Contributes to the improvement of data management processes on a global level.
Produces project-specific status reports for management and/or clients on a regular basis.
Provides training and work direction to junior staff as required.

Education and Experience Requirements:
Bachelors degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 0 to 2 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
Good written and verbal communication skills
Good analytical/problem-solving skills
Ability to maintain a high degree of confidentiality with clinical data and clients proprietary data
Strong customer focus and excellent interpersonal skills.
Proven flexibility and adaptability
Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands
Knowledge of medical/clinical terminology
Understands project protocol and DVM
Proven ability in achieving applicable technical competencies per the DM competency grid


Working Conditions and Environment:
Work is performed in an office environment with exposure to electrical office equipment.
Occasional drives to site locations
Occasional travel both domestic and international.

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.