Clinical Research Supervisor

START Center for Cancer Research•West Valley City, UT

1d•Onsite

About The Position

The Clinical Research Supervisor leads day-to-day clinical research operations at START, ensuring study conduct aligns with START standards, applicable regulatory requirements, and high-quality patient care. The role directs and oversees the Clinical Research Coordinator team and collaborates with Nursing, Data Coordination, Shared Services, and other support teams to support clinic operations, study activation, and quality activities. It is also responsible for department processes, staff training, recruitment support, retention, and supervision within the assigned area. The position is based at 5800 Foremost Dr SE, Grand Rapids, MI 49546, with a Monday–Friday schedule from 8:00 a.m. to 5:00 p.m. The work takes place in a very fast-paced and changing healthcare environment, with demanding deadlines and a continuing need to update knowledge. The role works closely with physicians and ancillary personnel caring for and treating oncology/hematology patients.

Requirements

Associate’s degree in health administration, nursing, or another related field.
At least 5 years of clinical research experience and 2 years of leadership experience in an oncology clinical research setting.
CITI GCP training.
Knowledge of GCP and applicable U.S. federal clinical research regulations.
Familiarity with Microsoft Office applications and clinical documentation systems.

Nice To Haves

Bachelor’s or master’s degree in health administration, nursing, or another related field.
Specialty certification in research or an associated field.
Demonstrated involvement in professional practice and industry advancement, such as conference attendance, poster presentations, or serving as a conference presenter or coordinator.
BLS certification.

Responsibilities

Provide proactive leadership and day-to-day oversight to the Clinical Research Coordinator team to support quality patient care and site-specific performance expectations.
Train, coach, and assess staff competency for assigned job responsibilities.
Ensure timely and accurate study documentation and communication with monitors and auditors; maintain compliance with GCP, applicable SOPs, and required training documentation.
Support study acquisition and activation in partnership with Shared Services, including participating in protocol review meetings and overseeing accurate site-level data collection and documentation in required systems.
Ensure efficient and compliant processes and systems support patient care and clinical research workflows.
Identify and implement practical process improvements that support patients, staff, and site operations.
Review incoming protocols for operational feasibility, focusing on coordinator workload, workflow, and site readiness.
Coordinate with Regulatory, Quality, Site Development, Pharmacy, Finance, and other support teams to promote compliant and effective study delivery.
Support effective use of the CTMS, EHR, and other required systems for accurate documentation and data capture within the assigned area.
Partner with site and department leaders to address operational issues and improve cross-functional workflows.
Support recruitment and retention within the assigned area.

Benefits

401(k) retirement savings plan with employer match.
Eligibility for an annual performance bonus, based on role and company results.
Paid time off and paid holidays.
Medical, dental, and vision coverage, with optional insurance options.
Company-paid life and disability insurance.
Employee Assistance Program providing confidential, no-cost support for employees and their families from day one.
Flexible FSA and HSA plans.
A supportive environment that values balance, wellbeing, and flexibility.
A collaborative workplace focused on continuous learning, professional growth, shared ideas, inclusivity, and innovation.

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