Senior Clinical Data Assoc

Job Description :

Work Schedule

Environmental Conditions

Senior Clin Data Assoc II

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 You ll 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 projects 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:

• Graduate or Postgraduate in Life Sciences.
• Previous experience that provides the knowledge skills and abilities to perform the job comparable to 4 to 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 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.