Associate Project Manager Oncology Jobs Vacancy at Covance Maidenhead
Covance Maidenhead urgently required following position for Associate Project Manager Oncology. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.
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Associate Project Manager Oncology Jobs Vacancy at Covance Maidenhead Jobs Details:
Assist in the cross-unit coordination both internal and external, inclusive of sub-contractors, for projects utilizing one or more Covance Services or sites.
Education / Qualifications
+ 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.
+ 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.
+ Working knowledge of Covance SOPs.
+ Experience as a Senior Clinical Research Associate, whether internal or external.
+ Minimum of four (4) years of relevant clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
+ In lieu of the above requirements, candidates with> five (5) years supervisory experience in a health care setting and four (4) years clinical research experience (including monitoring) in the pharmaceutical or CRO industries will be considered.
+ In lieu of the above requirements, candidates with five (5) years of site management and/or study/project coordinator experience will be considered.
+ 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 work with minimal supervision.
+ Good planning and organization skills.
+ Good computer skills with good working knowledge of a range of computer packages.
+ Excellent verbal and written communication skills.
+ Ability to set clear expectations for junior staff on projects.
+ 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.
+ I+ year additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
+ Local project coordination and/or project management experience.