Contract Conditions:
Start date: As soon as possible
Location: Europe (Remote)
Interviews: As soon as possible
Language: English, additional European Languages are a plus
Project: Neurology, Rare Disease
Key Responsibilities:
- Establishing and managing timelines, budgets, and resource plans for clinical trials.
- Coordinating and leading cross-functional teams, including investigators, CRAs, lead CRAs, and site coordinators.
- Ensuring precision in documentation, data entry, and adherence to regulatory standards.
- Fostering a collaborative and high-performing team environment.
- Addressing and resolving operational challenges during trial execution.
- Navigating unexpected issues while preserving the integrity of the study.
- Supervising CROs, laboratories, and other external vendors.
- Overseeing site selection, initiation, and ongoing monitoring activities.
Requirements:
- Strong experience (8-12 years) in Clinical Operations / Development within the biotech or - pharmaceutical industry.
- Experience in CNS studies is a plus.
- Exceptional written and verbal communication skills.
- Strong leadership and organizational skills, with a collaborative approach to teamwork.
If this role is of interest to you, please apply directly to learn more about the role. If not feel free to share with your network.
