Precision for Medicine are looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who have managed full service clinical trials within a CRO setting to join our global team.In this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology. Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.Involved luding proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.You will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team.How we will keep you busy and support your growth:You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentationsLiaise with Project Team and senior management of both Precision and sponsors, including C levelHandle and lead all aspects of a clinical research trial or trialsTotal project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trialsPrepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgetsRequirementsDegree or similar related life science qualification, or equivalent combination of education and experience.Previous experience in a full service/global Project Management role working in the CRO industry is essential.Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.Experience managing studies within OncologyWorking understanding of GCP/ICH guidelines and the clinical development processAbility to drive and availability for domestic and international travel including overnight staysBe able to communicate effectively in the English language both written and spokenStrong presentation skillsProven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)Proven ability to develop positive working relationships with individual and teams internally and externallyDemonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development planWe are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development.We invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.
10 days ago