
Senior Research Associate
6 days ago
This is a challenging position that requires expertise in ensuring the quality and integrity of clinical research studies.
The ideal candidate will have a deep understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements, as well as excellent communication and interpersonal skills.
Key responsibilities include:
- Conducting on-site and remote monitoring of clinical research studies to ensure compliance with GCP guidelines and regulatory requirements.
- Developing and implementing tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates.
- Contributing to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials.
- Managing defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues.
Requirements for this role include:
- A Bachelor's degree in a related field or equivalent experience.
- A minimum of 2-4 years of experience in clinical research monitoring.
- Strong knowledge of GCP guidelines and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and manage multiple priorities.
This is an exciting opportunity to develop your skills and contribute to the success of our organization. We offer a dynamic work environment, opportunities for professional growth, and a competitive compensation package.
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