Radiologist - Core Laboratory

Medpace, Inc.; Lyon; Sur place; EUR 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

Competitive compensation

Health and retirement benefits

WFH flexibility after training

Social events

Résumé du poste

Medpace is seeking a full-time, office-based Radiologist to join our imaging services team. You will perform blinded central radiology reviews and collaborate on protocol development for clinical trials, leveraging your imaging expertise and documentation accuracy.

The role requires MD licensure and radiology experience with various imaging modalities, along with proficiency in PACS and standard software. Office-based with on-site mentorship and ongoing training are provided.

Qualifications

• Must hold an MD and current medical licensure.
• Experience with imaging modalities and interpreting imaging studies.
• Familiarity with image analysis software (PACS) and quantitative assessments.

Responsabilités

• Complete source documents accurately and promptly per protocol.
• Perform blinded central radiology review according to study protocol endpoints.
• Review protocols and related study documents.
• Participate in training and competency development for central radiological review.
• Oversee assignments, training, and management of central reader.
• Participate in InterReader and InterReader variability assessments.
• Support sponsor site visits and audits as requested.
• Collaborate with management to resolve radiological and study-related concerns.
• Contribute to development, review and evaluation of SOPs and study procedures.
• Perform other duties as assigned.

Connaissances

MD licensure

Radiology experience

RECIST 1.1 knowledge

Formation

MD physician

Board Eligibility Radiology

Outils

PACS

Word

Excel

Access

Project

Description du poste

Job Summary

Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Radiologist to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

• Completing source documents accurately and promptly, according to the specific protocol requirements and Medpace's SOP
• Blinded independent central review of radiology examinations according to clinical study protocol endpoints as specified in study protocol, charter and according to GCP and standard Medpace SOPs
• Reviewing protocols, Image Review Charters and associated clinical and technical study documents as required
• Participating in training and subsequently demonstrating competency in the operation of independent central radiological review of imaging for clinical trials
• Participate in oversight of assignments, training, and management of central reader
• Participating in InterReader and InterReader variability assessments
• Participating in sponsor site visits and audits as requested
• Collaborating with management to resolve technical/radiological/study concerns and problems.
• Participating in the development, review and evaluation of SOPs and study specific procedures.
• Other duties as assigned

Qualifications

• Must have an M.D. and current medical licensure;
• Experience with most medical imaging modalities and expertise interpreting one or more imaging modality and therapeutic application
• Experience with various medical image analysis and viewing software (PACS) and use for quantitative image assessments
• Experience working with computer software including Word, Excel, Access and Project preferred
• Knowledge of radiological disease response criteria such as RECIST 1.1 preferred
• Board Eligibility in Radiology or equivalent training demonstrating competency

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
  • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• • Office based environment with on-site mentors
  • Defined career paths with clear advancement opportunities
  • Industry renowned onboarding and training programs designed to accelerate professional development
  • Ongoing training and continuous learning opportunities throughout your career
  • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• • Competitive compensation programs that recognize and reward performance
  • Comprehensive health, wellness, retirement, and PTO benefits
  • Office based culture with occasional WFH that provides flexibility for eligible positions after training
  • Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.