My client is looking for a Clinical Outcome Assessment Scientist to join their team for a 12 month contract starting in November.
The consultant would be based in one of two locations in France.
The consultant will be a part of a Clinical Outcomes team where they would work across the life cycle of drug development to generate patient insights about disease and treatment and develop measurement strategies to support development, post-
authorisation and commercial research activities.
Your responsibilities will include the following :
Generating an understanding of disease & treatment models through research
Examining patient insights on current treatments and perspectives on target product profiles
Advise on the development and use of instruments in clinical research projects
Conducting qualitative and quantitative research to influence development on disease models
Ensure correct and relevant input into medical evidence generation plans and effective implementation throughout execution including writing for certain parts of clinical trial protocols, statistical analysis plans and interpreting clinical outcomes assessment results from clinical trials.
Preparing abstracts and manuscripts
Identify and influence global external collaborations regarding policy, standards and uses of clinical outcomes assessments
Experience and Qualifications :
MSc in Health Economics, Epidemiology, Clinical Psychology, Public Health or Psychometrics
Training in Clinical Outcomes Assessment Methods
A minimum of 5 years’ experience in HEOR within the Pharma industry, CRO or Academia
At least 3 years’ experience working in Clinical Outcomes Assessment with a proven track record of disciplines including data analyses, scientific publications, input into clinical trials, peer-
reviewing, data synthesis etc.
Real World Evidence Experience
Fluency in English (oral and written)
Willing and able to travel globally