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Assistant Clinical Data Coordinator

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About the role

This vacancy has now expired. Please click here to view live vacancies.

SECTION 1: POSITION SUMMARY

 

Under supervision of more experienced Data Management Personnel and in accordance with project specific timelines, to perform basic data management activities to ensure the generation of accurate, complete, and consistent clinical databases. To fulfill his/her job responsibilities in accordance with Good Clinical Practices (GCPs), ICON Standard Operating Procedures (SOPs), Working Procedures (WPs), Study Specific Procedures (SSPs), International Committee on Harmonization (ICH) Guidelines, and all applicable laws and regulations

 

SECTION 2: JOB FUNCTIONS/RESPONSIBILITIES

 

. To learn to create local lab cleaning set-up documentation (e.g. mapping specifications)
. To learn to create and enter laboratory normal ranges in appropriate CDMS
. To learn to allocate the appropriate lab identifier in CRF CDMS
. To learn to review local laboratory data cleaning outputs
? To gain familiarity lab normal ranges, identifying the reason for outliers and take appropriate action as needed.
? To learn to resolve the issues with lab ID and Unit.
? To learn to generate data queries where applicable to resolve Lab discrepancies.
. Need to do Quality check for the Local Lab work
. Need to deliver the given project as per the given timeline
. To learn and maintain Local lab documentation within project files / study electronic directory as appropriate.
. To learn to complete any appropriate general or study specific planning tracker
. To learn to communicate with study team as appropriate
. Perform other duties reasonably related to the position as directed by manager/designee.

 

SUPERVISION

 

. N/A

 

SECTION 3: EXPERIENCE, SKILLS, KNOWLEDGE REQUIREMENTS

 

Previous Clinical Data Management experience is considered a plus but not required.
o Computer, keyboarding and word processing skills as relevant to the job function.
o Thorough knowledge of Lab reference ranges.
o Excellent understanding of medical terminology.
o Ability to read, understand, accurately interpret and follow procedures for all job related tasks.
o Excellent accuracy, attention to detail and capacity to maintain a high level of quality in local lab related tasks.
o Strong organizational and time management skills as to effectively organize workload to adhere to target metrics and complete all study related activities.
o Ability to work within a team environment and maintain a constructive approach when responding to internal and /or external customers as required.
o Ability to respond with flexibility to changing priorities in a fast paced environment.
o Ability to listen effectively.
o Professional and appropriate written and oral communication skills.
o Professional approach to the work environment.

EDUCATION REQUIREMENTS

 

Minimum of a Diploma or Degree in an appropriate Scientific discipline

 

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive salary and benefits package that includes an excellent pension scheme, private health care, life assurance and staff recognition schemes. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

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 - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.

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