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Full-Time Clinical Project Manager
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 a pro-active Project Manager to join our expanding CoSource team in Budapest.
About the job:
Essential Job Duties:
- Assist in the cross-unit coordination both internal and external, inclusive of sub-contractors, for projects utilizing one or more Covance Services or sites.
- Assist in the management and tracking of project resource needs and contribute to contingency planning for key resources.
- Assist in the successful design, implementation, tracking and revision of project plans for assigned projects.
- Assist in the leadership of the core project team, including CRAs, as directed by 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.
- Contribute to the effective teamwork among project team members within Covance departments and offices.
- Contribute to improvements to enhance the efficiency and the quality of the work performed on assigned projects.
- Meet/exceed client satisfaction expectations.
- Assist in ensuring that all staff allocated to assigned projects adheres to professional standards and SOPs.
- Provide performance feedback of team members to respective supervisors.
- Follow defined project issue escalation process and Covance’s Corrective Action Issue Resolution (CAIR) process.
- Under direction of SPM/PD, identify and assess risks and maintain associated documentation.
- Track client project metrics.
- Participate in internal project review meetings.
- Perform other duties as assigned by management
About you:
- University/college degree (life science preferred); in lieu of the above requirement, candidates with five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered.
- Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.
- Thorough understanding of the drug development process.
- Experience in managing global projects in a multi-office environment.
- Demonstrated ability to handle multiple competing priorities; utilize resources effectively.
- Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
- Demonstrated ability to lead by example and to encourage team members to seek solutions.
- Excellent communication, planning and organizational skills.
- Ability to work independently.
- Ability to negotiate and liaise with clients in a professional manner.
- Good computer skills with ability to understand and assess technology alternatives and implication for current processes.
- Comprehensive understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Comprehensive understanding of both site monitoring and study site management requirements.
- Comprehensive understanding of applicable regional regulatory requirements.
- Ability to understand and work with financial information.
- Ability to resolve project-related problems and prioritizes workload for self and team.
- Ability to work within a project team.
- Ability to work efficiently and effectively in a matrix environment.
THERE IS NO BETTER TIME TO JOIN US!
How to Apply
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