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Full-Time Associate Project Manager Study Start-up

COVANCE – Posted by apantov Budapest, Budapest, Hungary

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Job Description

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.

This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.

We are currently seeking an Associate Project Manager Study Start-up to join our expanding CoSource team in Budapest. This is an office-based position.

About the job:

• Assisting in the cross-unit coordination both internal and external, inclusive of sub-contractors, for projects utilizing one or more Covance Services or sites.
• Assisting in the management and tracking of project resource needs and contributing to contingency planning for key resources.
• Assisting in the successful design, implementation, tracking and revision of project plans for assigned projects.
• Serving as client primary contact for areas assigned by PM/SPM/PD.
• Assisting in the leadership of the core project team as directed by PM/SPM/PD to facilitate their ability to lead extended/complete project team including the maintenance of timelines in MS Project, creation of PowerPoint presentations and storyboards and maintenance and escalation of items in ADI log.
• Under direction of PM/SPM/PD, tracking project progress against financial milestones using applicable financial systems.
• Tracking client project metrics.

About You:

University/college degree (life science preferred), or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution.
• Previous relevant clinical research experience including demonstrated skills and competency in clinical project management tasks, especially regarding study start up.
• Comprehensive understanding of applicable regional regulatory requirements.
• Ability to work with minimal supervision.
• Good planning and organization skills.
• Ability to understand and work with financial information.
• Ability to resolve project-related problems and prioritizes workload for self and team.

THERE IS NO BETTER TIME TO JOIN US!

How to Apply

To apply please visit our career site www.covancecareers.com  quoting the reference 54752BR or follow the link: http://careers.covance.com/job-postings/54752BR/associate-project-manager-study-start-up  

Job Categories: Pharmaceutical. Job Types: Full-Time. Job Tags: budapest, clinical operations, clinical research, clinical sites services, Clinical trial, Clinical trial coordinator, CRO, EC submissions, English, Ethics Committee, GCP, GSS, ICH, office based, PM, project manager, RA, regulatory affairs, regulatory submissions, RSU, site feasibility, site selection, SOP, study feasibility, study protocol, Study start up activities, study start up associate, Study Start UP Project Manager, and study start up Specialist.

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