Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX

Medpace; Cincinnati (OH); On-site; USD 60,000 - 100,000; Full time

Job summary

Join a forward-thinking clinical research organization as an Associate Clinical Trial Manager, where you'll support project management activities in a dynamic team environment. This role is perfect for recent PhD graduates with a passion for oncology and hematology, offering comprehensive training and career growth opportunities. Enjoy a flexible work environment and competitive benefits while contributing to the development of innovative therapeutics. Be part of a dedicated team that values community and employee wellness, making a real difference in the clinical research field.

Benefits

Flexible work environment

Generous PTO starting at 20+ days

Competitive compensation and benefits

Employee events and wellness initiatives

Community involvement

Structured career development

Qualifications

• PhD required, preferably in Life Sciences.
• Strong presentation and communication skills are essential.

Responsibilities

• Communicate and collaborate on global study activities.
• Oversee regulatory filing systems and manage project timelines.

Skills

Project Management

Communication Skills

Organizational Skills

Presentation Skills

Fluency in English

Education

PhD in Life Sciences

Tools

MS Office

Job description

Associate Clinical Trial Manager - PhD - Oncology, Hematology, Radiopharm - Dallas, TX

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

Job Summary

Medpace is a leading CRO for biotech companies, seeking candidates with PhDs and/or Post-Doctoral Research experience in Oncology, Hematology, and Radiopharm for a full-time, office-based Associate Clinical Trial Manager (aCTM) role. The aCTM will support project management activities within the Clinical Trial Management team, working closely with Project Coordinators and Clinical Trial Managers. This role is ideal for recent PhD graduates eager to transition into industry, receive comprehensive training, and develop a career in clinical research and development of innovative therapeutics.

Responsibilities

• Communicate and collaborate on global study activities with project team members;
• Ensure timely and accurate completion of recurrent tasks;
• Maintain project-specific status reports in the clinical trial management system;
• Interact with internal teams, sponsors, study sites, and vendors;
• Oversee regulatory filing systems and study supplies;
• Create and manage project timelines;
• Coordinate meetings and produce minutes.

Qualifications

• PhD in Life Sciences;
• Fluency in English and strong presentation skills;
• Ability to thrive in a fast-paced, international environment;
• Experience in CRO or pharma industry is advantageous but not required;
• Proficiency in MS Office, organizational, and communication skills.

About Medpace

Medpace is a full-service clinical CRO providing Phase I-IV development services across various therapeutic areas, including oncology. Headquartered in Cincinnati, Ohio, with over 5,000 employees worldwide, our mission is to accelerate the development of safe and effective therapeutics.

Why Join Us?

Join Medpace to be part of a passionate team dedicated to making a difference. We offer a flexible work environment, competitive benefits, career growth opportunities, and a commitment to community and employee wellness.

Dallas Perks include:

• Flexible work environment
• Generous PTO starting at 20+ days
• Competitive compensation and benefits
• Employee events and wellness initiatives
• Community involvement
• Structured career development

Recognitions include being named a Top Workplace in 2024 and multiple CRO Leadership Awards.

Next Steps

Qualified candidates will be reviewed, and interested applicants will be contacted for further steps.