Cardiovascular Clinical Research Coordinator I

BioTecNika Global; Plano (TX); On-site; USD 52,000 - 66,000; Full time

Job summary

Baylor Scott & White Plano is seeking a Clinical Research Coordinator 1 to support cardiovascular trials from start to finish in a leading healthcare system. The role requires a Bachelor’s degree or 4 years of related experience, strong communication, and the ability to manage multiple studies while adhering to federal and institutional guidelines.

Responsibilities include coordinating protocols, interacting with PIs and regulatory staff, handling consent, monitoring visits, and ensuring

Qualifications

• Bachelor’s degree or 4 years of work experience.
• Proven written and oral communication skills.
• Ability to manage time-sensitive projects and establish effective working relationships.

Responsibilities

• Implements various protocols for assigned research projects with appropriate departments.
• Interacts with PIs, clinical managers, and supervisors.
• Creates, facilitates, or executes project workflows based on clinical trial protocol needs.
• Ensures appropriate billing mechanisms are in place for research charges.
• Performs research subject informed consent and entry into appropriate research studies.
• Partners and coordinates with regulatory compliance, preparing IRB materials and submitting IND Safety forms.
• Conducts and coordinates study-monitoring visits, audits, and quality checks.

Skills

Written & verbal communication

Time management

Relationship building

Education

Bachelor’s degree or 4 years of work experience

Job description

Baylor Scott & White Plano is seeking a Clinical Research Coordinator 1 to support cardiovascular trials from start to finish in a leading healthcare system. The role requires a Bachelor’s degree or 4 years of related experience, strong communication, and the ability to manage multiple studies while adhering to federal and institutional guidelines.

Responsibilities include coordinating protocols, interacting with PIs and regulatory staff, handling consent, monitoring visits, and ensuring