Empowering individuals to make a difference in the lives of others requires dedication, expertise and a passion for delivering exceptional results.
Clinical Trial Associate Role
The role involves providing clinical trial capabilities in support of clinical development. This includes ensuring investigator sites meet requirements to enroll study participants into clinical trials and supporting ongoing activities during site maintenance and close-out.
Key Responsibilities:
* Initiate and manage investigator site activities, including the collection and submission of regulatory documents, customization and negotiation of informed consent documents.
* Act as the primary point of contact for a site's ethics review board (ERB) and competent authority (CA) where applicable.
* Monitor and ensure site compliance with required training.
* Prioritize and effectively drive timelines aligned with company objectives.
Required Skills and Qualifications:
* Bachelor's degree preferably in a scientific or health-related field.
* In-depth understanding of the overall clinical development paradigm.
* Applied knowledge of project management principles and practices.
* Effective communication, negotiation and problem-solving skills.
Fluency in Romanian is essential for this role, with English language proficiency also highly valued. Relevant experience in clinical research and project management would be beneficial.