Real World Evidence - Contractor

Chiesi FarmaceuticiA•Cary, NC

1d•Hybrid

About The Position

Chiesi USA, based in Parma, Italy, is an international research-focused biopharmaceutical group with 90 years of experience, operating in 31 countries. With over 8,000 employees, the group is driven by the purpose of promoting a healthier world for people, patients, and the planet. Chiesi focuses on researching, developing, and marketing innovative drugs in key therapeutic areas, thinking generations ahead and driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behavior. As a Benefit Corporation and a certified B Corp, sustainability is embedded in its bylaws, and the company continuously measures its impact. Diversity, inclusion, and equal opportunity are central to Chiesi's identity, believing that differences strengthen the organization. It is a vibrant ecosystem of passionate individuals united by strong values and unique perspectives that challenge the status quo for the better. This role is for a motivated and detail-oriented contractor to support real-world evidence (RWE) research efforts. It is well-suited for recent PhD graduates with strong research skills and initiative. While guidance and mentorship are available, the ability to work independently and manage tasks effectively is essential. The contractor will contribute to key RWE projects, ensuring scientific rigor and timely execution. This is a 1-year contract position. Full-time availability is preferred, with a minimum of 30 hours per week required.

Requirements

PhD in epidemiology, health outcomes research, or a related field.
Strong analytical and problem-solving skills, with exposure to RWE methodologies and study design.
Ability to work independently, manage time effectively, and take initiative in problem-solving.
Proficiency in statistical programming (e.g., R, SAS, or Python) and experience working with healthcare data.
Strong communication skills, with experience in scientific writing and presenting research findings.

Responsibilities

Assist in the design and execution of RWE studies, including literature reviews, data analysis, and interpretation of findings.
Work with large healthcare datasets to generate insights that support regulatory, clinical, and commercial objectives.
Summarize and communicate findings through reports, presentations, and publications.
Collaborate with internal teams, external partners, and vendors to advance project goals.
Stay current with real-world data methodologies and regulatory considerations.