Global Clinical Operations Manager, Traveling CRC Team

Accel Research Sites

United States

Remote

USD 90,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Full-time benefits eligibility
Comprehensive benefits package

Job summary

Accel Research Sites is seeking a Clinical Operations Manager for its Traveling Team, based at Alcanza Corporate. You will coordinate clinical operations across multiple sites, ensuring patient safety, protocol compliance, and timely milestones.

The role requires strong project management and leadership to drive site performance, with up to 100% travel as needed. Collaboration with investigators, sponsors, and support teams is essential.

Qualifications

  • Associate's degree and a minimum of 3 years of clinical research experience, or an equivalent combination of education and experience.
  • 1+ years of management experience required.
  • Bi-lingual (English / Spanish) proficiency is a plus.

Responsibilities

  • Overall team management and support to enhance efficiencies, patient safety, and regulatory compliance.
  • Collaborate with Study Deliver, Operations, Strategy, and Training to coordinate delivery and milestones.
  • Oversee resourcing allocations, site assignments, and study team performance; identify risks and escalate as needed.
  • Assist with training for new and existing staff on clinical systems, SOPs, GCP, and guidelines.
  • Oversee site staff and conduct performance evaluations; manage timecards and onboarding.

Skills

Project management
Organizational skills
Communication
Risk mitigation
Multiple priorities
HIPAA compliance

Education

Associate's degree

Job description

Accel Research Sites is seeking a Clinical Operations Manager for its Traveling Team, based at Alcanza Corporate. You will coordinate clinical operations across multiple sites, ensuring patient safety, protocol compliance, and timely milestones.

The role requires strong project management and leadership to drive site performance, with up to 100% travel as needed. Collaboration with investigators, sponsors, and support teams is essential.

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