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: Project Coordinator
Job Description
· Plan and coordinate single service, standalone projects in accordance with the contract and in adherence with ICON SOPs, ICH GCP and appropriate regulations, and to liaise with other department managers as necessary to achieve this.
· Provide support to the Project Management Department and assistance to Project Manager(s) in completion of all required tasks to meet departmental and project goals as it relates to project document management requirements.
· Create, execute, maintain a detailed project plan in accordance with the approved scope of work and revise as appropriate to meet changing needs and requirements.
· Coordinate roles and responsibilities within the project team, ensuring that each team member understands requirements for project deliverables as outlined within the scope of work.
· Be the principal contact for Sponsors, especially as it relates to timelines, deliverables and financial objectives for the project, if required
Role Requirements / Skills / Experience Required
- Minimum BA/BS in the life sciences, nursing or related field or local equivalent.
- A minimum of one year of field monitoring experience or relevant clinical experience.
- A minimum of one year experience in the administration of Clinical Trials in a CRO environment or equivalent and/or one year project management training and comprehensive understanding of project management principles and applications.
- Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials
Additional Information:
Experience: 1 yrs
Qualification: BA/BS in the life sciences
Location: Chennai
Industry Type: Pharma
Functional Area: CRO
Last date: 23rd July, 2016
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