Current Jobs at PAREXEL

Key Accountabilities

• Organize and track delivery of all project documents as required
• Assist Medical Writers in all billable project-related tasks, as required. This includes assisting with client communication, set up and maintenance of project files and archiving.
• Provide administrative support, including coordination of meetings, recording and distribution of meeting minutes, photocopying, faxing, and maintenance of project trackers, as required.

Skills 

• Excellent interpersonal, verbal and written communication skills.
• Client-focused approach to work.
• A flexible attitude with respect to work assignments and new learning.
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
• Willingness to work in a matrix environment and to value the importance of teamwork.
• Knowledge of word processing, spreadsheet, database and e-mail applications desirable

Education

• Not specified but a primary degree, especially in health-related sciences, and/or an IT-related qualification would be an advantage.
• Consideration will be given to candidates who are technically sound along with experience of office administration.

Language Skills

• Fluent in written and spoken English.
• Minimum Work Experience
• Good knowledge of the Microsoft Office platform. Basic knowledge of general office practice

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Job Description

The Data Surveillance Analyst (DSA) provides leadership and expertise in all aspects of Data Surveillance and the set-up of support technologies, managing the delivery of all relevant data surveillance activities from Data Surveillance plan development and analysis tools setup through final Data Surveillance review.

What You'll Do At Parexel:

• Act as Data Surveillance Analyst, assess and review available study data to identify data quality trends, outliers, lack of variability, breeches of Quality 
• Support the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits, and central statistical analysis
• Apply working knowledge and judgment to identify and evaluate potential data quality issues. Determine and implement appropriate follow-up action with the input of other / relevant parties and / or guidance provided, if applicable.
• Provide feedback and work with Technology teams to identify potential solutions that match the business and technology strategy.
• Ensure timely and accurate review of Data Surveillance tools, systems and reports 

Ideal candidate will possess:

• Initial years of experience in clinical trials and programming knowledge in life science industry (CRO/Pharma/Academia).

Skills:

• Excellent analytical and problem-solving skills
• Understand data structure, (SDTM) data mapping
• Understand fundamentals of statistical data analysis.
• Basic SAS programming
• Strong oral and written communication skills.
• Strong presentation skills.
• Self-directed and ability to work independently in a virtual team environment.
• Strong time management skills, with ability to effectively prioritize and manage multi-project workload.
• Fluent in written and oral English Knowledge.

Education:

• Educated to a degree level (statistical, medical, clinical/health science, data management/analytics)