Senior Global Clinical Project Manager

​·        Title: Senior Global CPM - Vaccines

·        Location: Remote

·        Company: Mid-sized CRO (1000+ employees)

RBW Consulting is excited to announce a great opportunity to join one of our growing CRO clients. This company specialise in niche therapeutics including vaccines, rare diseases, ophthalmology, cell therapy, and neurology. After the acquisition of a vaccine-specific CRO and after winning studies in the vaccines space, they are looking for capable Senior Clinical Project Managers to support their global vaccines studies.

This company have a flexible approach and do not overwork their employees. The project management team is very friendly and rewards team accomplishments. Here, you will have a lot of visibility in the business and will have access to senior figures in the project team who can support you when required. It is also a very agile CRO where decisions can be made quickly without several layers of approval. Above all, they value transparency, quality of work, and collaboration.

Typical Responsibilities Include:

·        Provide strong, independent Clinical Operations leadership on assigned and/or complex projects

·        Communicate effectively and efficiently with clients, vendors, and internal team

·        Establish team roles and responsibilities and Provide clear direction to internal team and vendors to ensure study success

·        As 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 customers

·        Ensure projects are adequately staffed according to budget, SOW, and capabilities, and escalate to management when issues are present or anticipated that will require modifications

·        Manage protocol and ICF development as applicable

·        Oversee 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 staff

·        Design and implement study specific project plans, logs, and actions to keep project on track

·        Oversee and ensure delivery of timely project deliverables for all functional areas of the project

·        Ensure company or sponsor selected vendors are adequately supported from contracting through training /onboarding, and throughout the trial

·        Manage all study specific vendors contracts as applicable (per project scope and company contract scope)

·        Ensure adequacy of CRF design and development for the trial

·        Maintain project financial health through review of monthly activities against current SOW, and addressing change orders in a timely manner

·        Maintaining 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 needed

·        Assists in developing relationships with new and existing clients

·        Ensure 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:

·        At least 4+ years full service project management experience within CRO setting

·        At least 2 years’ experience in vaccines research as a Global CPM

To apply:

If you would like to discuss this vacancy further or to discuss your career options in confidence, please telephone on +44 (0) 1293 584 300

Please click ‘apply’ or contact Joe Pearce for any further information

About 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.