Director of Clinical Research

Priority Dispatch Corp.; Champaign (IL); Remote; USD 107,000; Full time

Job summary

An established industry player is seeking a Director of Clinical Research to lead a dynamic team in executing clinical trials. This role involves developing and implementing strategies to ensure high-quality outcomes while exceeding sponsor expectations. With a focus on leadership and mentorship, the ideal candidate will possess strong communication and organizational skills, along with a deep understanding of clinical research protocols and regulations. This position offers the flexibility of remote work with routine site visits, allowing you to balance professional responsibilities and personal commitments effectively. If you're passionate about advancing clinical research and fostering a collaborative environment, this opportunity is perfect for you.

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Disability Insurance

Life Insurance

Paid Time Off

Qualifications

• 5-8 years of experience in site management or clinical research.
• Deep understanding of drug development and FDA regulations.

Responsibilities

• Lead and manage a team of clinical research professionals.
• Ensure compliance and quality in clinical trial execution.

Skills

Leadership Skills

Communication Skills

Problem-Solving Skills

Data-Driven Decision Making

Organizational Skills

Education

Bachelor's Degree

ACRP or SOCRA Certification

Tools

Microsoft Office

Job description

Job Details

Job Location: 206 W WHITE STREET - CHAMPAIGN, IL

Position Type: Full Time

Salary Range: $106740.00 Salary/year

Description

JOB SUMMARY

The Director of Clinical Research is responsible for the development, implementation, and coordination of personnel supporting clinical trial operations for designated sites across Innovo’s site network. The role involves directing, planning, and coordinating clinical research activities to ensure goals and objectives are achieved within the prescribed timeframe and sponsor expectations. The director oversees recruitment, management, and retention of research staff. Experience in a clinical setting is preferred.

Responsibilities

The Director of Clinical Research is tasked with developing, implementing, and leading a team of highly skilled professionals to ensure successful execution of clinical trials. The focus is on achieving goals, exceeding sponsor expectations, and maintaining high standards of quality, compliance, and fiscal performance. The role also includes providing leadership and mentorship to the team and fostering a collaborative, growth-oriented environment.

• Lead and motivate a team of clinical research professionals across designated sites.
• Manage staff according to organizational policies and regulations, including planning, assigning, directing work, appraising performance, guiding professional development, and handling HR matters.
• Develop managers within the area to support staff career progression aligned with departmental and corporate priorities, overseeing regional talent development.
• Evaluate workload, quality, and performance metrics regularly, and initiate improvement plans for efficiency, quality, compliance, and financial performance.
• Ensure the Innovo site network meets performance metrics and provide solutions to meet expectations when needed.
• Implement risk management strategies to identify and address operational, timeliness, and quality issues proactively.
• Oversee staffing, resource planning, training, quality assurance, and site evaluations across clinical trial projects.
• Report regularly to program leadership, review quality assurance reports, and develop corrective action plans.
• Perform other related duties as required.

Qualifications

• Bachelor's Degree or equivalent experience required.
• Must be ACRP or SOCRA certified.
• 5-8 years of relevant experience in site management, development, or expansion.
• Clinical experience preferred.
• Ability to travel as necessary (5-10%).
• Deep understanding of drug development, GCP/ICH, FDA regulations, and guidelines.
• Knowledge of clinical research financial parameters, CTMS, billing, and accounting.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in Microsoft Office.
• Strong organizational and problem-solving skills.
• Effective time management with the ability to multitask.
• Data-driven decision-making skills.
• Ability to establish effective working relationships.

Benefits (for full-time)

• Competitive salary
• Health, dental, vision, disability, and life insurance
• Paid time off

Working Conditions

This role operates remotely with routine site visits. Standard office equipment is used. Flexibility in hours is allowed, with core hours from 9:30 a.m. to 3:30 p.m. and a 37.5-hour workweek. Occasional evening and weekend work may be required.

All statements are intended to describe the general nature of work. More detailed information can be found in SOPs, policies, and guidelines. Innovo Research is committed to equal employment opportunity and a discrimination-free workplace. All employment decisions are based on business needs, job requirements, and individual qualifications, without discrimination. Reasonable accommodations will be provided for qualified individuals with disabilities.

Applicants must be authorized to work in the U.S. without sponsorship, as Innovo cannot sponsor visas at this time.