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Work as QA Administrator in Icon Clinical Research

 

Clinical courses

ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.

Post: QA Administrator

Job Description
- You will effectively provide administrative support to the Quality assurance department especially the QA Management system (iQ)
- iQ Administration support which includes managing the QA and non QA user login accounts and manage project entry to iQ.
- Reporting- regular and adhoc reports for QA management, sponsors and other departments etc.,
- QA Audit support- create, assign and update records as required, create observation records and assist with creation of audit templates.
- QC- perform regular reviews of iQ data to check for inconsistencies and work with QA teams to correctand update records, as needed.
- General QA administration- perform some basic administration tasks for the QA team as needed including organising,scheduling, facilitating meetings etc., and assist in completion of departmental and project goals. Assist with coordination of external audits hosted by the QA department.

Candidate Profile
· Bachelor’s degree in life sciences, business administration or local equivalent qualification/relevant work experience.
· Prior relevant work experience in Quality assurance, Regulatory or other relevance administrative support experience would be ideal.
· Excellent organizational, verbal and written communication skills.
· Strong technical skills, including proficiency in MS Office applications with strong skills in excel.
· Ability to prioritize, multi task and work independently with time sensitive material.
· Able to work independently in a global matrix environment. A strong team player, flexible in work time, if business requires.
· Meticulous attention to detail and excellent customer service skills.
· Thorough understanding of management confidentiality(in relation to both project and personnel information).
· Strong communication skills, both written and oral.
· Ability to produce reports to a high standard will be advantageous.
· Fluency in English is essential.


Additional Information:
Location: Bangalore
Reference: 012384
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QA
End Date: 10th February, 2015

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