We are seeking a skilled Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for conducting site visits and monitoring the progress of clinical trials.
The ideal candidate will have a strong background in clinical research, with experience in conducting site visits and monitoring trial compliance. You should also have excellent communication and interpersonal skills, as well as the ability to work independently and as part of a team.
Responsibilities:
* Conduct site visits to monitor trial progress and ensure compliance with study protocols
* Collaborate with site staff to resolve any issues or concerns that may arise during the course of the trial
* Prepare and submit reports on trial progress and compliance
* Participate in audit preparation and follow-up activities as needed
Requirements:
* Bachelor's degree in a life science or related field
* At least 2 years of experience in clinical research, preferably in a site management or monitoring role
* Excellent communication and interpersonal skills
* Able to work independently and as part of a team
What We Offer:
* A competitive salary and benefits package
* The opportunity to work with a dynamic and experienced team
* Ongoing training and professional development opportunities
If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity.