Regional Director, Clinical Operations
Title:
Regional Director Clinical Operations Location:
Detroit, MI Hours/Schedule:
40 hours/week Type:
Direct HireWe are looking for a Permanent Regional Director of Clinical Operations for the Detroit, MI Region.
If you want to be a part of this groundbreaking work, please apply!Responsibilities Lead, Manage and Hold Accountable (LMA) Provide overall leadership and support for clinical research sites within their region, assisting site directors and coordinators.
Develop and executes an operational strategy to achieve business objectives.
Management of multiple regional sites, development and revision of policies and procedures.
Train directors to ensure sites are run effectively.
Complete regular director evaluations.
Identify and explore ways to control cost and generate revenue.
Drive Enrollment Ensure efficient operations of each site in their region, including enrollment goals being met and site operating procedures are being followed.
Feasibility Oversight Feasibility support for business development team.
Manage Clinic Relationships Serve as a resource to Investigators and Site Directors on feasibility assessments, compliance, and best practices.
Establish good working relationships and collaborative arrangements with principal investigators and office administration to help achieve the goals of the organization.
Partner with the VP of operations and other senior leaders to ensure that all site locations are equipped with strong leadership.
Expected to provide back-up or emergent need for the clinical research coordinating team.
Create a culture of being proactive versus reactive.
Ensure ongoing competence of site directors and staff.
Quality Control Develop, manage, and report on key data and metrics.
Requirements Bachelor's degree in health-related field and/or successful completion of formal clinical training program (e.
g.
, EMT, RN, MA).
Medical background (RN, PA, MT, EMT) degrees preferred with clinical research experience required and can be used in lieu of degree.
Management experience, and clinical research coordination experience.
Personality to work in a dynamic environment; always leading by example.
Highly self-motivated and able to operate autonomously.
Strong communication skills, and experience communicating within the study site as well as among the site and sponsor, clinical/contract research organization (CRO), and regulators.
Formulate business decisions that are financially responsible, accountable, justifiable, and defensible.
Detail-oriented and excellent with metrics.
Data-driven and critical thinking skills to continuously improve approaches that achieve the goals as quickly as possible.
Ability to work flexible hours and/or overtime to meet study deadlines and requirements.
Knowledge of all components of the research process as it pertains to clinical trials.
Ability to work at more than one site, travel to participating clinics and attend off-site staff meetings, conferences.
Regular and punctual attendance.
Perform other duties as assigned.
Travel RequirementsOccasional travel may be required in this position Recommended Skills Assessments Attention To Detail Business Development Business Planning Clinical Research Clinical Research Coordination Estimated Salary: $20 to $28 per hour based on qualifications.
Regional Director Clinical Operations Location:
Detroit, MI Hours/Schedule:
40 hours/week Type:
Direct HireWe are looking for a Permanent Regional Director of Clinical Operations for the Detroit, MI Region.
If you want to be a part of this groundbreaking work, please apply!Responsibilities Lead, Manage and Hold Accountable (LMA) Provide overall leadership and support for clinical research sites within their region, assisting site directors and coordinators.
Develop and executes an operational strategy to achieve business objectives.
Management of multiple regional sites, development and revision of policies and procedures.
Train directors to ensure sites are run effectively.
Complete regular director evaluations.
Identify and explore ways to control cost and generate revenue.
Drive Enrollment Ensure efficient operations of each site in their region, including enrollment goals being met and site operating procedures are being followed.
Feasibility Oversight Feasibility support for business development team.
Manage Clinic Relationships Serve as a resource to Investigators and Site Directors on feasibility assessments, compliance, and best practices.
Establish good working relationships and collaborative arrangements with principal investigators and office administration to help achieve the goals of the organization.
Partner with the VP of operations and other senior leaders to ensure that all site locations are equipped with strong leadership.
Expected to provide back-up or emergent need for the clinical research coordinating team.
Create a culture of being proactive versus reactive.
Ensure ongoing competence of site directors and staff.
Quality Control Develop, manage, and report on key data and metrics.
Requirements Bachelor's degree in health-related field and/or successful completion of formal clinical training program (e.
g.
, EMT, RN, MA).
Medical background (RN, PA, MT, EMT) degrees preferred with clinical research experience required and can be used in lieu of degree.
Management experience, and clinical research coordination experience.
Personality to work in a dynamic environment; always leading by example.
Highly self-motivated and able to operate autonomously.
Strong communication skills, and experience communicating within the study site as well as among the site and sponsor, clinical/contract research organization (CRO), and regulators.
Formulate business decisions that are financially responsible, accountable, justifiable, and defensible.
Detail-oriented and excellent with metrics.
Data-driven and critical thinking skills to continuously improve approaches that achieve the goals as quickly as possible.
Ability to work flexible hours and/or overtime to meet study deadlines and requirements.
Knowledge of all components of the research process as it pertains to clinical trials.
Ability to work at more than one site, travel to participating clinics and attend off-site staff meetings, conferences.
Regular and punctual attendance.
Perform other duties as assigned.
Travel RequirementsOccasional travel may be required in this position Recommended Skills Assessments Attention To Detail Business Development Business Planning Clinical Research Clinical Research Coordination Estimated Salary: $20 to $28 per hour based on qualifications.
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