Clario. The Best of ERT & Bioclinica.In anticipation of our 2022 growth plans, we're eager to share this opportunity and connect with you now.Consider joining Clario's Cardiac Safety PM team as a Project Manager! This person will be responsible for directing/managing services for client projects to assure high quality, on-time and on-budget services while promoting excellent customer service.Clario delivers the leading endpoint technology solutions for clinical trials. Through experience gained from over 19,000 clinical trials delivered in support of 870 regulatory approvals, Clario fuses scientific expertise and global scale into the broadest endpoint technology platform to enable pharmaceutical, biotech and medical device partners to transform lives. Through Trial Anywhere, Clario has mastered the ability to generate rich evidence across all trial models: decentralized, hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe and Asia Pacific, Clarios global team of science, technology and operational experts has been delivering the richest clinical evidence for nearly 50 years.
In this role you will:Lead the Planning and Setup, Monitoring, and Closeout phases of Cardiac Safety study managementMonitor study timelines and manage the financial components of each studyIdentify potential study risks and mitigations, and escalate as appropriate.Manage internal/external negotiations and promote collaboration to foster a positive team environment, effective communications, and efficient use of resources to meet study timelines and contractual obligations.Apply problem solving strategies to address customer issues and maintain issue tracking documentation to monitor progress and ensure timely resolution to customer escalationsEnsure compliance with timely training completion and documentationPresent study services at Investigator Meetings or site initiation meetings as neededAttend client meetings with Business Development and/or Operational teams to present Company services and Operational Data flow, as neededAssist with training new members of the Project Management team and perform other duties, assignments, or special projects as time and/or circumstances necessitate.The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. This job description and any attachments do not constitute or represent a contract.
What we seek:Bachelor Degree and/or proven demonstrated Project Management skills or experience within the industryAt least 2-4+ years of experience in pharmaceutical field (or related industry experience), with an emphasis on project management. Prior clinical trial research and a good understanding of study protocol will be very helpful!Excellent organizational, interpersonal, time management, and prioritization skillsExcellent verbal and written communication skills, including ability to communicate effectively in EnglishWorking knowledge of Microsoft Office productsKnowledge of the pharmaceutical drug development processDetail oriented and demonstrated responsiveness to inquiries and requestsValid passport and ability to travel approximately 20%What we offer:Competitive Salary plus Annual bonus targetExcellent Onboarding planGlobal Exchange ProgramPMP Certification supportExceptional Tuition Reimbursement programComprehensive Benefits Package, including a generous paid time off program and a flexible work from home policyWe are an equal opportunity employer and all qualified applicants receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Join us!#LI-DNI