Clinical Data Associate (US/Remote)

Requisition Number: 3881

Position Title: Clinical Data Associate

External Description:

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. 

We are Worldwide Clinical Trials, and we are a global team of almost 2,500 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. 

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. 

Data Management is an ever growing and collaborative department! Our global team is a group of diverse individuals with wide-ranging experience within the industry. From start to finish, we are involved in clinical studies beginning with building the study database, to locking and delivering the final dataset for the project. Data Management reviews and ensures the clinical study data is of high quality for regulatory submissions.

The Data Management group is the perfect place to launch or further your career. Whether it is technical expertise, or coming from a clinical background, you’re able to hone and expand your skillset within our department. Spanning various roles from data support staff, database and SAS programmers, coders and functional leads, there is place for you!  

The Clinical Data Associate will support the Data Manager in the management and processing of clinical data, within assigned projects to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor’s satisfaction.

RESPONSIBILITIES:
Tasks may include but are not limited to:

• To assist the Data Manager in all data cleaning activities.
• To assist the Data Manager with the preparation of trial documentation.
• To perform verification and User Acceptance Testing of configured databases.
• To assist the Data Manager with the creation and validation of Manual and SAS checks.
• To assist the Data Manager with the reconciliation of data from external sources (e.g. Serious Adverse Events, IVRS, Central Laboratory)
• Responsible for the registration of users into the EDC/CTMS system, performing system demonstrations if required.
• To assist with the maintenance of procedure logs, coding schemes, input notes and Data Entry Manuals.
• To coordinate the arrival and logging of data sheets using in-house software and data entry systems.
• To conduct components of Database Quality Assessments on the clinical databases as requested by the Data Manager.
• To establish and/or maintain correspondence files with participating centres.
• Archiving of trial documentation and (e)CRFs. 
  Perform other duties as assigned.  The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
   

OTHER SKILLS AND ABILITIES:

• The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.
• It is essential that the job holder works with close attention to detail and is questioning about the validity of the data being entered and has an ability to phrase data queriesin an understandable and impartial manner.
• To have the ability to train new staff and to monitor their performance

REQUIREMENTS:

• Educated to degree level (preferably Life Science), Nursing qualification, or relevant industry experience 

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Employment Type: Regular

Community / Marketing Title: Clinical Data Associate (US/Remote)

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

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