Clinical Research Operations Lead

McKesson Corporation; Dallas (TX); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Total Rewards package

Annual bonus opportunities

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Manager Clinical Research Support to supervise clinical support operations at the Dallas clinic. You will ensure regulatory compliance, optimize workflows, and lead a multidisciplinary team across research assistants, program managers, and coordinators.

The role emphasizes patient safety, data integrity, and SOP development in a fast-paced oncology research environment with a competitive Total Rewards package.

Qualifications

• Associate's degree in clinical research, healthcare, or related field obtained.
• 1+ years' work experience in clinical trial operations including regulatory, safety, and biospecimen management.
• Expertise in GCP, GLP, HIPAA, OSHA, and IATA regulations.
• Experience in research protocol interpretation and clinical trial management systems.
• Advanced experience in MS Office and EMR; proficient in clinical trial databases.

Responsibilities

• Provide direct supervision and mentorship for support staff and coordinators.
• Oversee and optimize clinical support including biospecimen collection, processing, and documentation per protocol and regulatory requirements.
• Coordinate collection of vital signs, ECGs, and lab specimens with data integrity.
• Ensure patient safety and confidentiality across clinic and research activities.
• Develop and monitor SOPs and align with corporate and regulatory guidelines.

Skills

GCP

GLP

HIPAA

OSHA

IATA

EMR

MS Office

EDC

Education

Associate's degree in clinical research

Bachelor's degree preferred

Tools

Clinical trial databases

Excel

Word

SharePoint

PowerPoint

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Manager Clinical Research Support to supervise clinical support operations at the Dallas clinic. You will ensure regulatory compliance, optimize workflows, and lead a multidisciplinary team across research assistants, program managers, and coordinators.

The role emphasizes patient safety, data integrity, and SOP development in a fast-paced oncology research environment with a competitive Total Rewards package.