
Clinical Research Specialist
4 hours ago
Job Summary
We are seeking a Clinical Research Associate to conduct on-site and remote monitoring of clinical research studies, ensuring compliance with widely accepted clinical practices.
This role involves developing and implementing tools, procedures, and processes to guarantee quality monitoring.
The successful candidate will contribute to the design, implementation, and delivery of processes, programs, and policies, including SOPs and training materials.
Responsibilities include managing defined components of projects or processes within the area of responsibility.
Additionally, this role requires documenting monitoring activities and findings accurately and timely, as well as collaborating with cross-functional teams to support clinical trial operations.
]Requirements
- Bachelor's degree in a related field or equivalent experience.
- Minimum of 2–4 years of experience in clinical research monitoring.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Excellent communication and interpersonal skills; ability to work independently and manage multiple priorities.
Certifications
Certified Clinical Research Associate (CCRA) or equivalent certification preferred.
Necessary Skills
- Attention to detail, strong analytical, and problem-solving skills.
- Ability to work effectively in a team and manage time.
- Strong organizational and time management skills; proficiency in Microsoft Office Suite.
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