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Clinical Research Operations Manager

Be Well Clinical Studies
Round Rock, TX Full Time
POSTED ON 2/27/2023 CLOSED ON 9/17/2023

What are the responsibilities and job description for the Clinical Research Operations Manager position at Be Well Clinical Studies?

Seeking an experienced Clinical Operations Manager (COM)

  • Preferred minimum of 5 years experience as a Clinical Research Coordinator (CRC)
  • Position requires strong project management and organizational skills
  • Ability to work collaboratively in a team setting

Clinical Operations Manager supports, facilitates, and coordinates the daily trial activities, playing a critical role in the trials. The COM is responsible for managing the trials, staff, and facility. Responsibilities include, but not limited to:

  • Overseeing the trouble-free running of clinical trials, mitigating issues
  • Following and enforcing SOPs
  • Project management of studies
  • Lead coordinate and manage by example
  • Collecting data obtained from research, coding and analyzing it
  • Managing budgets set aside for research and the department
  • Communicating with volunteers regarding study objectives
  • Liaising with Physicians and laboratories regarding research findings
  • Monitoring the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards
  • Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
  • Directing the collection, labeling, storage, and transport of all specimens
  • Ensuring that all equipment and supplies needed for the study are in-stock and in good working order
  • Meet with study Monitors
  • Create an environment (culture) for your team to thrive.
  • Ensure staffing and schedule is covered daily/monthly/quarterly
  • Facility maintenance, organization and upkeep
  • Timeclock management for your department
  • Staff training and assignments
  • Maintain on-site presence to assist with subject consent questions and vaccination/infusion safety.
  • Maintain Training, including CITI/GCP, and study specific training for the duration of each study
  • Other duties as assigned.

Qualifications:

  • 4-year college degree preferred
  • Degree optional if at least 5 years of experience as Clinical Research Coordinator

Job Type: Full-time

Pay: $60,000.00 - $75,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Flexible schedule
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • Monday to Friday

Experience:

  • clinical research: 6 years (Preferred)

Work Location: One location

Salary : $60,000 - $75,000

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