Senior Clinical Research Associate Job Opportunity
This is an exceptional chance to join our team as a Senior Clinical Research Associate. As a key member of our clinical development group, you will play a pivotal role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
Key Responsibilities:
* Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
* Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
* Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
* Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
* Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Requirements:
* Complete bachelor's degree in life sciences, nursing, or medicine.
* Strong previous experience as a Clinical Research Associate I and II, with a strong understanding of clinical trial processes and regulatory requirements.
* Previous experience with ONCOLOGY studies.
* Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
* Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
* Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
We offer competitive compensation packages, annual bonuses, health-related benefits, and retirement plans. Our culture rewards high performance and nurtures talent. We strive for a workplace free of discrimination and harassment.