Senior Clinical Trial Manager – Remote

Medpace; United States; Remote; USD 80,000 - 120,000; Full time

Job summary

An established industry player in clinical research is seeking a Clinical Trial Manager to oversee operations in a dynamic environment. This role involves managing day-to-day project activities, ensuring compliance with regulations, and leading cross-functional teams. The ideal candidate will have extensive experience in clinical trial management, particularly within a CRO setting, and possess strong leadership skills. Join a forward-thinking organization dedicated to improving patient outcomes through innovative clinical development. This is a unique opportunity to make a significant impact in the healthcare field while advancing your career in a supportive and flexible work environment.

Benefits

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualifications

• 5+ years as a project/clinical trial manager within a CRO required.
• Experience in Phases 1-4; Phases 2-3 preferred.

Responsibilities

• Manage day-to-day operations of the project according to ICH/GCP.
• Serve as primary Sponsor contact for operational project issues.
• Develop operational project plans and manage study vendors.

Skills

Leadership Skills

Project Management

Clinical Trial Management

Risk Assessment

Education

Bachelor’s degree in a health-related field

Advanced degree in a health-related field

Job description

Our activities in South America are expanding! Medpace is the leading CRO for Biotech companies and we are seeking to add an established Clinical Trial Manager to join our Clinical Trial Management Group in Chile. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus programs along with local benefits.

Responsibilities

• Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
• Serve as primary Sponsor contact for operational project-specific issues and study deliverables
• Maintain in depth knowledge of protocol, therapeutic area, and indication
• Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
• Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Manage study vendors where applicable
• Manage site quality and monitoring deliverables

Qualifications

• Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
• Experience in Phases 1-4; Phases 2-3 preferred
• 5+ years as a project/clinical trial manager within a CRO required
• Management of overall project timeline
• Bid defense experience preferred
• Strong leadership skills

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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