Job Summary
A growing mid-sized, global Contract Research Organisation (CRO) is seeking a Clinical Research Associate II/III to join its team onsite in the United States. This role is central to the delivery of agile and patient-centered clinical development solutions, contributing to advancements in scientific research.
Responsibilities
- Collaborate with potential investigators and institutions to discuss and establish study budgets.
- Support the conduct of clinical trials through effective management and oversight of study processes.
- Ensure compliance with regulatory requirements and company standards during research activities.
- Assist in the documentation and monitoring of clinical trial progress and results.
- Engage in the preparation and review of study protocols and other essential documents.
Qualifications
- Experience in clinical research as a Clinical Research Associate, preferably at the II/III level.
- Relevant educational background in sciences, nursing education, or a healthcare-related field.
- Proven ability to effectively collaborate with multiple stakeholders in the clinical trial process.
- Strong knowledge of regulatory requirements and best practices in clinical research.
- Excellent organizational and communication skills to manage study logistics and documentation.
Optimapharm d.o.o. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
