Senior Clinical Research Associate (Oncology)

PRA International; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

PRA International is looking for a Senior Clinical Research Associate to oversee and manage clinical trials, ensuring compliance and data integrity. This role involves monitoring sites, conducting visits, and training site staff. If you have extensive CRA experience and strong problem-solving skills, we invite you to apply.

Qualifications

• Extensive experience as a Clinical Research Associate.
• Strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects.

Responsibilities

• Monitor clinical trial sites for adherence to protocols and regulations.
• Conduct site visits to assess performance and resolve issues.
• Collaborate with teams for accurate data collection and reporting.

Skills

Organizational skills

Problem-solving skills

Communication skills

Interpersonal skills

Stakeholder management

Monitoring practices

Data integrity

Education

Advanced degree in life sciences, nursing, or medicine

Tools

Clinical trial software

Job description

Overview

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

Responsibilities

What You Will Be Doing:

• 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.

Qualifications

Your Profile:

• Advanced degree in a relevant field such as life sciences, nursing, or medicine highly preferred.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• 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.