Location: Europe, Middle East & Africa-Netherlands-Utrecht-Z
Closing Date: 25 Feb 17
Type: Full Time
Salary (£): On Application
PPD has an exciting opportunity for a Clinical Team Manager (CTM) join us onsite exclusively for one of our strategic pharmaceutical partners, office based in Zeist, the Netherlands. PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD. ...
PPD has an exciting opportunity for a Clinical Team Manager (CTM) join us onsite exclusively for one of our strategic pharmaceutical partners, office based in Zeist, the Netherlands. PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD.This is a great opportunity for study managers/CTM’s or those with relative experience working within the life science sector for pharmaceutical, biotech companies or CRO’s industry who would enjoy the opportunity to work for a CRO dedicated to one client. The role coordinates all aspects of clinical activities on an international basis. Responsible for the local implementation of local clinical trials and entrusted to them, their preparation for their closure, in compliance with GCP, regulatory requirements, SOPs, quality standards, deadlines and costs. This could include oversight of the Clinical Research Associates who are allocated to a project on a Country basis. You will work in partnership with the relevant stakeholders to ensure the necessary training, tracking and quality systems are in place for the clinical team, and be primarily responsible for the clinical deliverables of the Project within agreed timelines and budget. Clinical Team Managers provide contact and support to the project sponsor for all clinical aspects. We are seeking high performing individuals who enjoy a fast-paced environment and have had Clinical Management experience OR exposure to local studies, involving the coordination of CRAs. With your excellent written and oral English skills you will have exceptional interpersonal and problem solving skills, with the ability to lead CRAs in different countries. You will also have proficient working knowledge of GCP and experience in several medical / therapeutic areas. You must be comfortable working in a matrix management system and have the ability to motivate, mentor and integrate teams. We are seeking highly motivated and skilled applicants who will want to share in our continued growth in the international market place. We will consider field based applicants depending on your experience level. PPD is a leading global contract research organization providing drug discovery, development, lifecycle management, laboratory services and outsourcing solutions. PPD is a leading global CRO providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to help clients and partners bend the cost and time curve of drug development to deliver life-changing therapies that improve health. For more information, visit www.ppdi.com. *LI-JP1
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