Clinical Trial Project Manager - Oncology/Hematology

Medpace; Cincinnati (OH); Hybrid; USD 80,000 - 110,000; Full time

Job summary

An established industry player in the clinical research field is seeking a Clinical Trial Project Manager specializing in Oncology/Hematology. This role involves managing daily project operations, ensuring compliance with regulations, and serving as the primary contact for sponsors. The company offers competitive salary and bonus packages, along with flexible work arrangements. Join a team dedicated to improving patients' lives through innovative clinical trials and enjoy a collaborative environment that values professional growth and community involvement.

Benefits

Flexible Work Arrangements

Competitive Benefits

Professional Growth Opportunities

Community Involvement

Employee Perks

Qualifications

• 5+ years of project/clinical trial management experience within a CRO.
• Experience in Phases 1-4 clinical trials, with a focus on Phases 2-3.

Responsibilities

• Manage daily project operations and ensure accountability.
• Serve as the primary Sponsor contact for operational issues.
• Oversee internal project team members and deliverables.

Skills

Clinical Trial Management

Project Management

Leadership Skills

Risk Assessment

Education

Bachelor's Degree in Health-related Field

Advanced Degree

Job description

Clinical Trial Project Manager - Oncology/Hematology

Job Locations
United States-OH-Cincinnati | United States | United States-TX-Irving (Dallas) | United States-CO-Denver

Job Summary

Medpace is a leading CRO for biotech companies, expanding our Clinical Trial Management Group with experienced Clinical Trial Managers and Project Managers specializing in Oncology/Hematology. We have recently expanded our Cincinnati campus and have offices in Dallas and Denver, offering remote flexibility for qualified candidates. We provide competitive salary/bonus packages and equity grants that are highly lucrative for our associates.

Responsibilities

• Manage and ensure accountability for daily project operations, in accordance with contracts, ICH/GCP, and applicable laws and regulations.
• Serve as the primary Sponsor contact for operational issues and study deliverables.
• Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
• Oversee internal project team members and deliverables, ensuring all necessary training is provided.
• Review and contribute to study protocol, edit check specifications, data analysis plan, and final report.
• Develop operational project plans.
• Manage risk assessment and execution.
• Handle study vendor management.
• Manage site quality, supervise Clinical Research Associates, and monitor deliverables.

Qualifications

• Bachelor's degree in a health-related field; an advanced degree is preferred.
• Experience in Phases 1-4 clinical trials; Phases 2-3 preferred.
• At least 5 years of project/clinical trial management experience within a CRO, with home-based management required.
• Strong leadership skills and experience managing project timelines.

Medpace Overview

Medpace is a full-service CRO providing Phase I-IV clinical development services to biotech, pharma, and medical device industries. Our mission is to accelerate the development of safe, effective therapeutics through a disciplined scientific approach, leveraging expertise across all major therapeutic areas. Headquartered in Cincinnati, Ohio, with over 5,000 employees across more than 40 countries.

Why Medpace?

Join us to make a difference. We value people, purpose, and passion, with a focus on improving patients' lives. Our Cincinnati campus offers flexible work, competitive benefits, and professional growth opportunities, along with community involvement and employee perks.

Awards include being named a Top Workplace in 2024 by The Cincinnati Enquirer and recognition by Forbes and Life Science Leader magazine.

Next Steps

A Medpace team member will review your application, and if interested, you will be contacted for further steps.

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