Clinical Research Manager Jobs

About The Position

Requirements

• Bachelor's degree
• At least 3 years of experience directly related to the duties and responsibilities specified
• Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.

Nice To Haves

• Strong knowledge of clinical research principles, regulatory requirements, and patient care standards
• Experience managing clinical research teams and complex study operations
• Proficiency in budgeting, resource allocation, and fiscal management
• Experience with data systems, reporting tools, and research documentation
• Knowledge of clinical procedures, and patient care protocols
• Experience with grant development and research funding processes
• Excellent interpersonal, leadership, and communication skills
• Ability to manage competing priorities and make sound decisions in a fast-paced environment
• Strong organizational and problem-solving abilities
• High level of professionalism when handling sensitive and confidential information
• Ability to design and implement systems for data collection, tracking, and analysis

Responsibilities

• Lead the planning, development, and implementation of clinical trial protocols, procedures, and operational systems in collaboration with the Principal Investigator
• Oversee day-to-day clinical trial activities to ensure efficient workflow, protocol adherence, and high-quality patient care
• Establish and manage data collection systems; oversee the accurate collection, processing, and reporting of clinical data and specimens
• Recruit, supervise, train, and evaluate clinical research staff
• Ensure all clinical and research activities comply with protocol requirements, clinical standards, and safety regulations
• Set priorities, manage workloads, and foster a collaborative, high-performing team environment
• Oversee participant recruitment, screening, enrollment, and retention strategies
• Provide direct patient care and perform clinical procedures as appropriate
• Educate research participants on study protocols, treatments, and investigational products
• Develop and manage study budgets, resource plans, and operational needs
• Coordinate procurement and setup of clinical facilities, equipment, and supplies
• Maintain database that contains records related to patient incentives, inventory, and study documentation
• Ensure compliance with all applicable federal, state, and institutional regulations
• Maintain complete and accurate source documentation and study records
• Prepare reports and communicate study progress, outcomes, and patient responses to investigators, sponsors, and regulatory bodies
• Serve as a liaison between investigators, departments, sponsors, and regulatory agencies
• Support audits, identify operational challenges, and implement corrective actions
• Contribute to grant writing, funding proposals, and long-term research planning
• Represent and promote research initiatives to internal and external stakeholders

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• Life insurance
• Educational benefits through the tuition remission and dependent education programs