Project Manager- CARDIOVASCULAR

What the Project Manager does at WorldwideThe Project Manager (PM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. WCT Project Managers are 100% accountable for the success of their projects.Project Manager (PM) is responsible for the overall coordination and management of clinical trials from start up through close out activities.Directs the technical, financial and operational aspects of the projects -- thus securing the successful completion of clinical trials.Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented.Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations *The PM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.What you will doLead core project team members and facilitate their ability to lead extended/complete project teamLead cross unit coordination both internal and external, inclusive of sub-contractorsDefine and manage project resource needs in conjunction with functional heads and establish contingency plans for key resourcesEnsure successful design, implementation, tracking and revision of project plans for assigned projectsPromote effective teamwork among project team members; resolve conflicts as neededEnsure appropriate communication on project-related matters with the PM ManagementWhat you will bring to the roleExperience in managing projects in a multi-office environmentDemonstrated ability to handle multiple competing priorities; utilize resources effectivelyDemonstrated ability to inspire effective teamwork and motivate staff within a matrix systemDemonstrated ability to lead by example and to encourage team members to seek solutionsExcellent communication, planning and organizational skillsSelf-motivated and excellent problem solving skillsYour experienceUniversity/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilitiesMinimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasksIn lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries will be considered and/or proven ability and demonstration of relevant experience and skills in clinical developmentThorough knowledge of project management processesThorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programsAvailable for domestic and international travel, including overnight staysValid current passport requiredAbility to drive and have a valid driver’s licenseFluent in local office language and in English, both written and verbalBroad knowledge of drug development process and client needs