Impact-Driven Clinical Research Operations Manager

McKesson’s Corporate; Dallas (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Manager of Clinical Research Support for our Dallas, TX clinic. This onsite leadership role supervises Lab Research Assistants and Clinical Research staff, manages biospecimen collection and documentation, and drives SOP development to meet regulatory standards.

You will oversee operations, ensure patient safety and data integrity, and coordinate with protocol requirements in a fast-evolving clinical trial environment.

Qualifications

• Associate degree in clinical research or healthcare, Bachelor’s preferred.
• 1+ years in clinical trial operations with GCP/GLP/HIPAA/OSHA/IATA knowledge.
• Experience interpreting protocols and using trial management systems.
• Proficient in Microsoft Office and EMR systems.
• Familiar with clinical trial databases and EDC.

Responsibilities

• Provide supervision and mentorship to support staff.
• Oversee clinical support, biospecimen handling, and documentation.
• Coordinate collection of vital signs, ECGs, and specimens with protocol adherence.
• Maintain patient safety and confidentiality across activities.
• Develop and monitor SOPs aligned with guidelines.

Skills

Clinical trial operations

Regulatory compliance

EMR experience

Data integrity

Education

Associate's degree in clinical research, healthcare, or related field

Bachelor's Degree

Tools

Microsoft Office Suite

EMR systems

Clinical trial management systems

Electronic data capture

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Manager of Clinical Research Support for our Dallas, TX clinic. This onsite leadership role supervises Lab Research Assistants and Clinical Research staff, manages biospecimen collection and documentation, and drives SOP development to meet regulatory standards.

You will oversee operations, ensure patient safety and data integrity, and coordinate with protocol requirements in a fast-evolving clinical trial environment.