About This Role
We are seeking a highly motivated and detail-oriented Clinical Research Associate to conduct on-site and remote monitoring of clinical research studies.
Key Responsibilities:
* Conduct thorough on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
* Develop and implement tools, procedures, and processes to guarantee quality monitoring.
* Manage defined components of projects or processes within your area of responsibility.
* Utilize practical knowledge of a professional area, typically obtained through education combined with experience.
* Maintain high standards of clinical practice and ensure the success of clinical trials.
Qualifications and Skills:
* 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.
* Proficiency in using clinical trial management systems and other relevant software.
Necessary Competencies:
* Attention to detail and strong analytical skills.
* Problem-solving abilities and critical thinking.
* Ability to work effectively in a team environment.
* Strong organizational and time management skills.
* Proficiency in Microsoft Office Suite.
Certification Preferred:
* Certified Clinical Research Associate (CCRA).