Clinical Data Lead

If you have a background in clinical data management combined with the experience of creating edit checks, developing data delivery specifications, data management plans, and reports, learn more about how you can be a part of growing Clinical Research Organization that offers continued growth in the field of Data Management.  

About the Clinical Data Lead role within ICON: 

The Clinical Data Lead will be responsible for ensuring on time project management of trial aspects from the Data Management Group.  The Project Data Lead will represent Data Management at Kick-off, Charter and SRS team meetings and review and provide input into Charter and SRS during creation.

The Clinical Data Lead will partner with Database Administrators (DBA), SAS Programmers and System Development to coordinate and code delivery in accordance with specification and work with DBA, SAS Programmers and System Validation team to ensure test data is acceptable and meets requirements of test plan, work with Systems Development on database structure and code lists, and work with Sponsors and/or CROs to develop Data Delivery Specifications (DDS).

It will be the role of the Clinical Data Lead to ensure clinical data is tracked, entered, cleaned and stored with accuracy and integrity and provide feedback to the Project Management team and Client. Will create project specific edit check documents and work with DBAs to create, test and implement.  Will perform quality review of incoming clinical data, coordinate the loading of clinical data, assist in maintaining database documentation, implement quality control procedures, and investigate and analyze discrepancies in data and report to DBA.

Benefits of working at ICON:

We provide our Clinical Data Leads with the resources to be successful in supporting their line of business. In addition, we offer a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and an annual incentive plan to reward performance.  

To succeed you will need:

You will have a Bachelors degree or local equivalent along with a minimum of 2 years of Clinical Data Management.  You project management experience along with a strong analytic ability.  Have good documentation, organizational, and communication skills.  Experience in data definition and mapping is helpful along with familiarity interpreting requirements per protocol.

Must have knowledge and familiarity with EDC systems and SAS and SQL experience is a plus.  Training in computerized systems in clinical trials, Software Development Life Cycle, and computerized systems in clinical research is ideal.

We invite you to review our opportunities at www.iconplc.com/careers.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.

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