Senior Global RWE Study Lead Job Description
This role involves overseeing various aspects of real-world evidence studies. The successful candidate will have at least 2 years of experience in study management and will be responsible for managing a portfolio of studies.
Responsibilities
* Oversee the entire lifecycle of RWE studies, from initiation to closure
* Manage and coordinate with cross-functional teams, including research scientists, statisticians, and data analysts
* Analyze and interpret complex data sets to inform study design and methodology
* Develop and maintain high-quality documentation and reports for sponsors and regulatory authorities
Requirements
To be successful in this role, you will need:
* A degree in a life science or related field (e.g., biology, chemistry, pharmacology)
* At least 2 years of experience in study management, preferably in a clinical trials setting
* Strong analytical and problem-solving skills, with the ability to work effectively under pressure
* Excellent communication and interpersonal skills, with the ability to collaborate with internal and external stakeholders
* Familiarity with regulatory requirements and industry standards (e.g., ICH, GCP)
What We Offer
This role offers flexible working options, which may include remote work arrangements. You will also have opportunities to develop your skills and knowledge through ongoing training and professional development programs.