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Clinical Outcomes Associate Consultant
3 months ago
We are looking for a Clinical Outcomes Associate Consultant to play a pivotal role in project teams by delivering analytical insights, leadership, and innovative solutions to client engagements, business development initiatives, and internal projects.
The Clinical Outcomes Associate Consultant will be responsible for defining project scopes, constructing work plans, and formulating comprehensive and valuable conclusions and recommendations for our clients. This position is essential in ensuring that we equip our clients with the insights and information necessary for their success.
This role primarily focuses on two rapidly expanding sectors of the consulting field: Clinical Outcome Assessment:
• Engage in projects aimed at the development, assessment, and application of Clinical Outcome Assessments research, including Patient Reported Outcomes.
• Provide research assistance across all facets of project execution, encompassing qualitative and quantitative data collection, data analysis, report composition, and the drafting of abstracts and manuscripts.
About You – qualifications, education, skills, and achievements.
• A master's degree in health psychology, psychology, sociology, life sciences, or a related field (a 2:1 or higher).
• A minimum of 12 months of experience in outcomes research, qualitative research, and/or the development and evaluation of patient-reported outcomes.
• Proficient in the MS Office suite, including Excel, PowerPoint, and Word.
• At least 6 months of experience working collaboratively in a team setting (either vocational or academic).
It would be advantageous if you also possess:
• A PhD.
• Familiarity with clinical drug development and regulatory (FDA, EMA) guidelines and procedures.
• Insight into the pharmaceutical/medical device industry and the operational environment of clients.
• Exceptional verbal and written communication skills.
• Experience with Atlas, NVIVO, or MAXQDA.
• Capability to manage multiple projects and prioritize tasks effectively.
• Strong time management, organizational skills, and attention to detail.
• A diligent work ethic with a commitment to delivering high-quality results.
• The ability to work independently and proactively, addressing problems as they arise.
Responsibilities in this role include:
• Project Execution
o Conduct research to produce consistently high-quality deliverables with minimal oversight, including:
o Develop qualitative and quantitative research study protocols, including interview guide and survey creation.
o Lead and perform literature and instrument reviews, including the formulation of search strategy protocols, citation screening, literature review, data extraction table development, and social media data analysis where applicable.
o Plan and execute reviews of relevant COA/PRO instruments in accordance with scientific and regulatory standards.
o Conduct competitor landscape analyses, such as reviewing PRO labels, EPARs, approved FDA and EMA labels, and regulatory meeting documentation.
o Organize and conduct qualitative interviews/focus groups with patients, clinicians, caregivers, and other pertinent stakeholder groups.
o Provide research guidance and support to research analysts.
o Prepare reports and present findings (Word/PowerPoint).
o Extract key messages from data analysis and formulate recommendations.
o Attend and present at client meetings.
o Participate in training as required.
• Collaborate with project teams to meet deadlines and achieve project goals.
• Ensure effective and timely administration in accordance with established styles and processes.
About the Team:
Our team comprises 18 health psychologists and outcomes researchers with extensive methodological and commercial expertise. We specialize in the design, validation, and implementation of patient-reported outcome (PRO) and other COA instruments for clinical trials and clinical practice, focusing on FDA and EMA guidelines, as well as HTA bodies. Our experience spans various therapeutic areas, including oncology, immune disorders, respiratory conditions, psychiatry, CNS, autoimmune diseases, infectious diseases, pain management, and women's health. We are supported by a global multi-disciplinary team, including medical writers, health economists, systematic reviewers, and strategic advisors as needed. Together, our experts deliver integrated health economics and outcomes research (HEOR) and market access solutions throughout the product life cycle.
Work Hours:
This is a full-time permanent position requiring hybrid work arrangements. The role necessitates weekday attendance with some flexibility around core working hours.
Employee Benefits:
Private Medical Insurance or Health Cash plan. Generous Pension Plan contribution rates. Income protection insurance. Life insurance. Sports Club Subsidy (Company pays 50% of gym membership, or up to £500). Emergency Childcare or Adult care cover. Eyecare vouchers. From 25 Days Annual Leave + 8 Bank Holidays (option to buy and sell Annual leave).At Clarivate, we are dedicated to providing equal employment opportunities for all individuals concerning hiring, compensation, promotion, training, and other employment terms and conditions. We adhere to applicable laws and regulations governing non-discrimination in all locations.
