Associate, Coa

2 months ago

London, United Kingdom Clarivate Full time

We are looking for an Associate to join our Clinical Outcome Assessment (COA) Consulting team.

In this role, you will work on COA consulting projects and will conduct research to produce high-quality deliverables with mínimal guidance.

If you have experience in outcomes research, qualitative research and/or patient reported outcomes development and evaluation, we would love to speak with you.

About You - experience, education, skills, and accomplishments.- Master’s degree in health psychology, psychology, sociology, life sciences or other relevant topic.- At least 12 months experience in outcomes research, qualitative research and/or patient reported outcomes development and evaluation.- Previous experience with MS office suite including Excel, PowerPoint, and Word

It would be great if you also had...- At least 6 months experience working in a team (either vocational or academic).- PhD- Understanding of clinical drug development and regulatory (FDA, EMA) procedures and guidance- Knowledge of the pharmaceutical/medical device industry and the clients operating environment- Previous experience in Atlas, NVIVO or MAXQDA

What will you be doing in this role?- Conducting. Conduct research to produce consistently high-quality deliverables.- Developing. Develop qualitative and quantitative research study protocols including interview guide development, and survey development.- Achieving. Work with project team to meet project deadlines and achieve project objectives.- Leading. Lead and conduct literature and instrument reviews including development of search strategy protocols, citation screening, literature review, development of data extraction tables, and review of social media data where appropriate.- Planning. Plan and conduct qualitative interviews/focus groups with patients, clinicians, caregivers, and other relevant stakeholder groups. Plan and conduct reviews of relevant COA/PRO instruments according to scientific and regulatory guideline

About the Team- The teams you work with are primarily located in EMEA, and you may work with teams internationally in the US and APAC.- The COA team helps 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 18 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, Lead 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 Work

This is a full-time permanent position based in London, UK and will require hybrid working in our Liverpool Street office (2-3 days per week in office, rest of week remote).

This position requires weekday (Monday - Friday) attendance with some scheduling flexibility available around core working hours.

LI-Hybrid, #LI-Onsite

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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