SENIOR GLOBAL CLINICAL PROJECT MANAGER - VACCINES

Title: Senior Global CPM - VaccinesLocation: RemoteCompany: Mid-sized CRO (1000+ employees)Salary: €75,000 - €90,000 plus other benefits (depending on level of experience)RBW Consulting are delighted to announce an exciting opportunity on behalf of one of our close clients. This company is a full-service CRO with global offices across North America, APAC, and Europe. They are currently in an expansion phase after the acquisition of two niche CROs in both Eastern and Western Europe. They are truly one of the most exciting growing CROs in globally right now and cover a wide range of therapeutic areas. Recently, they have won new business in the vaccine space and have exciting global studies to support in this area of their business.The Senior Global CPM will become a natural leader within the department. They will be expected to have hands-on experience managing global trials within vaccine studies at a high level. They will be client-facing and will actively support in developing request for proposals with biopharmaceutical clients, selecting suitable staff, creating BID language, and developing milestones in accordance to agreed timelines and budgets. They may also be expected to take on a strategic role with the client if required.This is a great opportunity to network with an expanding company and the Head of Global Project Management who is creating a talented team of Global Project Managers. It is also a great chance to become an early leader within a growing department and contribute towards interesting vaccines research.Typical Responsibilities Include:Provide strong, independent Clinical Operations leadership on assigned and/or complex projectsCommunicate effectively and efficiently with clients, vendors, and internal teamEstablish team roles and responsibilities and Provide clear direction to internal team and vendors to ensure study successAs primary contact with clients and vendors, establishing communication mechanism and formats that meet the needs of all parties supporting the trial in development and strategizing on any proposals or bids to external customersEnsure projects are adequately staffed according to budget, SOW, and capabilities, and escalate to management when issues are present or anticipated that will require modificationsManage protocol and ICF development as applicableOversee and ensure company site selection process is successful through oversight of feasibility questionnaire development, management of workflow, and reviewing record of processes managed by the assigned clinical staffDesign and implement study specific project plans, logs, and actions to keep project on trackOversee and ensure delivery of timely project deliverables for all functional areas of the projectEnsure company or sponsor selected vendors are adequately supported from contracting through training /onboarding, and throughout the trialManage all study specific vendors contracts as applicable (per project scope and company contract scope)Ensure adequacy of CRF design and development for the trialMaintain project financial health through review of monthly activities against current SOW, and addressing change orders in a timely mannerMaintaining scope change log and execution Change Orders / Budget Amendments as needed.Prepare and maintains project financial workbook each month, including forecasting updates from study start through closure with ongoing review of data during trials, as neededAssists in developing relationships with new and existing clientsEnsure team members are adequately trained on the project to perform their assigned tasks and services.Ensure data deliverables are complete and current throughout the trial through regular review of data management reports, review of monitoring activities, and site management reports (as applicable)Mentor / coach junior team members as needed to support their success as well as to ensure the trial success. This level of support may include support / attendance at select Site Qualification, Site Initiation, Interim and Close-out Visits, and may be especially important for early phase trials to support client expectations.Requirements:Life science degree or equivalentAt least 4+ years full service project management experience within CRO settingAt least 2 years’ experience in vaccines research as a Global CPMTo apply:If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 1293 584 300Please click ‘apply’ or contact Joe Pearce for any further informationAbout RBW Consulting:RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients. We give back by playing an active role in funding initiatives that change lives. We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.We are an equal opportunities Recruitment Business and Agency:RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.