Site Manager
Há 5 dias
We are seeking a dedicated CRA to support clinical trial execution and ensure successful site management.
Key Responsibilities:- Conduct on-site visits, develop subject recruitment strategies, and deliver training to site personnel.
- Evaluate site performance, address quality concerns, and maintain compliance with regulatory standards.
- Monitor study progress, gather essential documents, and document site activities.
- Collaborate with cross-functional project teams to facilitate study execution and align with project goals.
This role requires at least 1 year of on-site monitoring experience and a strong understanding of GCP, ICH guidelines, and regulatory requirements.
RequirementsTo succeed in this position, you should possess the following skills and qualifications:
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong attention to detail and organizational skills.
Familiarity with GCP, ICH guidelines, and regulatory requirements is a must. Additionally, proficiency in MS Office applications, particularly Excel, is highly desirable.
BenefitsAs a Clinical Research Associate, you will have the opportunity to work on various projects, develop your skills, and advance your career in the field of clinical research. You will also have access to ongoing training and professional development programs to stay up-to-date with industry trends and best practices.
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