As a Clinical Research Coordinator, you will play a vital role in planning, executing, and managing clinical trials. You will oversee project timelines, budgets, and resources, while ensuring compliance with FDA regulations and guidelines.
Responsibilities
Design and implement operational plans for clinical trials.
Oversee the integrity and quality of study data.
Identify opportunities for process improvements within the study framework.
Facilitate communication among cross-functional teams involved in the trials.
Ensure timely recruitment of study participants and tracking of outcomes.
Assist in the preparation of protocols, consent forms, and other study materials.
Engage with external vendors for services needed in clinical trials.
Review and approve study-related expenses.
Prepare presentations and reports for stakeholders regarding trial progress.
Support compliance audits and inspections as required.
Requirements
Education
Bachelor's degree in life sciences or related field
Master's degree in a healthcare-related field is preferred
Experience
5-7 years of experience in clinical research or project management
Technical Skills
Data Management
Regulatory Compliance
Soft Skills
Analytical Thinking
Problem Solving
Certifications
Good Clinical Practice (GCP) Certification
Certification in Clinical Research (ACRP)
Languages
English: Fluent
Advantageous
PMP Certification: Preferred for project management expertise.
Experience in oncology or other therapeutic areas: Specific experience in relevant therapeutic areas is valued.
Benefits
Comprehensive health benefits
401(k) plan with competitive matching
Professional development programs
Employee wellness initiatives
Company Culture
Innovative Practices: We embrace innovation and seek forward-thinking solutions in our work.
Inclusive Atmosphere: We value inclusivity and diversity in our workforce and celebrate unique backgrounds.
Work-Life Balance: We prioritize a healthy work-life balance, providing flexible options for our employees.