Clinical Research Coordinator B

Manage phases of complex clinical trials under general supervision, ensuring compliance with good clinical practice and coordinates with partnering institutions, supports monitoring of external sites, and participates in study and protocol training meetings.

Requirements

• Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
• A Master's degree is preferred.
• Excellent interpersonal and communication skills.
• Strong attention to detail and ability to maintain accurate records.
• Ability to communicate effectively, both verbally and in writing, with individuals from diverse backgrounds and professional levels.
• Strong organizational skills with the ability to manage multiple tasks and meet deadlines under tight timelines.
• Experience working collaboratively on a research team and interacting with study participants.
• Proficiency using computer programs for research operations (MS Office Suite, REDCap, Asana, email programs).
• Experience with data analysis programs is preferred.

Benefits

• Excellent healthcare
• Tuition benefits
• Generous retirement benefits
• Professional development opportunities
• Supportive work and family benefits
• Health and wellness programs and resources