Clinical Research Coordinator

Benefits

• Dental insurance
• Free uniforms
• Health insurance
• Paid time off
• Vision insurance
• Life insurance

The Clinical Research Coordinator plays a pivotal role in the management and execution of clinical trials. This position involves coordinating all aspects of clinical research studies, ensuring compliance with regulatory standards, and maintaining the integrity of data collected throughout the trial process. The ideal candidate will possess a strong understanding of clinical development and be adept at managing documentation and data management tasks while adhering to HIPAA regulations.

Pre Med students encouraged to apply.

• Coordinate and oversee clinical trials from initiation through completion, ensuring adherence to study protocols and timelines.
• Conduct patient assessments, including taking vital signs and collecting clinical laboratory samples as needed.
• Review and manage documentation related to clinical research activities, ensuring accuracy and compliance with regulatory standards.
• Maintain up-to-date knowledge of clinical research practices, regulations, and standards to ensure compliance throughout the study process.
• Collaborate with cross-functional teams, including investigators, sponsors, and regulatory bodies to facilitate successful trial execution.
• Ensure participant confidentiality by adhering to HIPAA guidelines in all aspects of research activities.

• Bachelor’s degree in a relevant field such as life sciences or healthcare; advanced degrees are a plus.
• Previous experience in clinical research or related fields is highly desirable.
• Strong understanding of clinical trials, data management, and documentation review processes.
• Familiarity with clinical development standards and regulatory requirements governing clinical research.
• Excellent analytical skills with attention to detail in data collection and reporting.
• Strong communication skills, both verbal and written, with the ability to work collaboratively in a team environment.
• Proficient in using electronic data capture systems and other relevant software tools for managing clinical research data.

This position offers an opportunity to contribute significantly to the advancement of medical knowledge through rigorous scientific inquiry while working within a dynamic team environment dedicated to improving patient outcomes.

Job Type: Full-time

Experience:

Clinical Research : 1+ year (Required)

Work Location:

In person