Note: The job is a remote job and is open to candidates in USA. Trinity Life Sciences is committed to enhancing life sciences commercialization through innovative strategies. They are seeking a Consultant to support their Evidence, Value, Access, and Pricing teams with various research activities, including literature reviews and value dossier development.
Responsibilities
- Conduct general secondary research activities such as review of clinical guidelines, epidemiology sources, treatment algorithms, product’s reimbursement status across key markets
- Perform literature data search from multiple databases, including PubMed and EMBASE
- Execute review of selected publications, including quality control with second reviewer, while being able to extract relevant data
- Perform statistical analysis for the meta-analysis based on the feasibility assessment
- Perform meta-analysis based on data quality and availability, including plot generation (*nice to have*)
- Utilize research and review findings to lay the foundation for value dossier development
- Review and analyze previous value dossiers, while developing draft value frameworks, and adapting these at the regional and local level
- Analyze and synthetize primary and secondary research data to feed into the development of a value dossier and related guidance / tool-kit materials
- Support execution of primary research programs (e.g., focus groups, IDIs) to pressure test, inform value story development, and exploring opportunities to investigate value proposition from competition
Skills
- Bachelor's degree with high academic achievement; major in health sciences, Economics, HEOR, and/or demonstrated interest in life sciences is a plus
- 2.5+ years of research experience in consulting, research organizations or related fields – medical writing background preferred
- Strong oral and written communication skills in English language
- Ability and knowledge in use PubMed/ Medline, Google Scholar, other literature research platforms
- Proficiency in MS Office Suite (Microsoft Word, PPT, and Outlook); Foundational knowledge of MS Excel is required
- General understanding of systematic review methods, clinical research design, and applicable standards and regulations for clinical trials
- Medical writing background preferred
- Perform meta-analysis based on data quality and availability, including plot generation (*nice to have*)
Benefits
- In addition to your base salary, you will also be eligible for an annual discretionary performance bonus.
Company Overview