Job Overview:
We are seeking a seasoned clinical research professional to join our team as a Senior Clinical Research Associate. In this role, you will be responsible for conducting on-site monitoring at various locations, ensuring compliance with study protocols and managing site activities.
Key Responsibilities:
* Conduct on-site monitoring visits at designated locations
* Ensure compliance with study protocols and Good Clinical Practice (GCP)
* Manage site activities and resolve any issues that may arise
* Perform documentation reviews and ensure accuracy of records
* Collaborate with cross-functional teams to ensure seamless execution of studies
Requirements:
* Bachelor's degree in Life Sciences or related field
* At least 5 years of experience in clinical research, preferably in Oncology or Hemophilia trials
* Excellent communication and organizational skills
* Strong understanding of clinical trial procedures and regulations
* Ability to work independently and collaboratively as part of a team
What We Offer:
This role offers the flexibility to work remotely from anywhere with internet access. We provide a competitive salary and benefits package, as well as opportunities for growth and development.
Why Join Us?
We are committed to delivering high-quality results and exceeding client expectations. Our team is passionate about making a difference in people's lives through clinical research.
If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.