We are looking for a Director, Consulting to join our Consulting team in the UK. This role is working on COA consulting projects. The team consists of 100 technical experts and is reporting to the Senior Director, Consulting. We have great skill set in consulting for Patient Reported Outcomes/Clinical Outcomes Assessment and we would love to speak with you if you have skills in line management and training.About you – experience, education, skills, and accomplishments Master’s degree in health psychology, psychology, sociology, life sciences or other relevant topic10 years’ experience in Patient Reported Outcomes/Clinical Outcomes Assessment including building:In-depth knowledge and experience of clinical outcomes assessments, patient reported outcomes, development and validation of outcome measures, and clinical trial endpoint strategyIn-depth knowledge and experience of the pharmaceutical industry and the clients operating environment (regulatory and HTA)At least 8 years’ significant consulting experience in a client facing role and ability to instil confidence and convey authority with colleagues and clientsDemonstrated ability to lead multiple complex projects and project teams consecutively It would be great if you also had . . . Experience of line management and trainingExperience of financial managementDemonstrated business development experienceDemonstrated thought leadership experienceWhat you will be doing in this role?Providing. Provide high level, technical expertise and strategic input and advice to clients.Leading. Lead team of COA analysts providing technical domain training and guidance in US and EU regulatory guidance for PRO/COA endpoints, qualitative, quantitative, and mixed methods research methods and analysis within a COA context, literature and instrument reviews, clinical trial endpoint reviews and development and validation of PRO endpoints for product labelling claims and facilitating market access.Contributing. Contribute significantly to the attainment of yearly revenue/profit targets, business development, and proposal writing.Providing. Provide strategic advice that demonstrates understanding, experience and authority by offering effective solutions to meet client needsIdentifying. Identify and develop new business opportunities with new and existing clientsDeveloping. Develop and maintain a strong external presence within the external COA communityAbout the teamThe COA team help pharmaceutical sponsors to select, develop, and validate clinical outcomes assessments (patient-reported outcome measures, clinician-reported outcome measures, observer-reported outcome measures, and performance outcome measures) for use in clinical trials for new treatments. We work across many different therapy areas. We sit within Evidence, Value, and Access (EVA) in Clarivate.The COA team comprises 15 COA specialists who primarily run primary and secondary research studies focused on selecting, developing, and/or validating COAs. A typical project for us may start with a targeted literature review and then move onto a qualitative interview study with patients, caregivers, and clinicians. We also support our sponsors in their regulatory strategy and communications. Our consulting projects require an inquisitive mind, strong research skills, and an understanding of industry guidance e.g., FDA PRO Guidance for Industry and Patient Focused Drug Development Guidance. The team are COA specialists at various stages of their career. The team includes Associates, Associate Consultants, Consultants, Senior Consultants, Directors, and Senior Directors. All the team are strong researchers with an industry understanding and commercial focus, working towards the common goals of measuring what matters to patients. The team has grown substantially in recent years and comprises diverse skill sets.The team are collaborative, hardworking, and value our work-life balance. We work together in a supportive environment where the aim is to deliver high quality research that meets our clients’ needs and ultimately improves outcomes for patients.Hours of workThe teams you work with are primarily located in EMEA, and you may work with teams internationally in the US and APAC. This is a full-time permanent role.At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.
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