Clinical Research Associate II Role
A leading clinical research organization is seeking a highly skilled Clinical Research Associate II to manage site qualifications and monitoring throughout clinical trials. The ideal candidate will be responsible for ensuring compliance with GCP/ICH guidelines, assisting with site activities, and maintaining accurate documentation.
The successful candidate will hold a relevant degree and possess strong communication and interpersonal skills. They should be able to travel regularly and work effectively in an inclusive workplace environment.
* Ensure compliance with GCP/ICH guidelines.
* Assist with site activities.
* Maintain accurate documentation.
The role requires strong organizational and problem-solving skills, as well as the ability to work independently and collaboratively as part of a team. Travel is expected up to 75% of the time.
Key Responsibilities:
* Conduct on-site visits to monitor and maintain quality control.
* Develop and implement site qualification plans.
* Collaborate with cross-functional teams to ensure trial timelines are met.
Requirements:
* Bachelor's degree in a life science or related field.
* Minimum 2 years of experience in clinical research.
* Strong communication and interpersonal skills.
* Ability to travel up to 75% of the time.
We offer a competitive salary and benefits package, as well as opportunities for career growth and professional development. If you are a motivated and detail-oriented individual looking for a challenging role in clinical research, please apply today.