Physician Reviewer - Radiology

Medpace, Inc.

Heverlee

Sur place

EUR 90 000 - 150 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Competitive pay
Health benefits
Retirement plan
WFH flexibility
Social events

Résumé du poste

Medpace seeks a full-time, office-based Radiologist to join our imaging services team. You will perform independent central radiology review and ensure protocol compliance for clinical trials.

The ideal candidate holds an MD with medical licensure, expertise across imaging modalities, and experience with PACS and RECIST criteria. This role offers a collaborative environment, on-site mentoring, and ongoing professional development.

Qualifications

  • Must have an M.D. and current medical licensure.
  • Experience with most medical imaging modalities and interpreting imaging.
  • Familiarity with PACS and quantitative image assessments.
  • Word, Excel, Access and Project experience preferred.
  • Knowledge of RECIST 1.1 criteria preferred.
  • Board Eligibility in Radiology or equivalent training.

Responsabilités

  • Complete source documents accurately per protocol and SOPs.
  • Blinded central review of radiology exams per study protocol.
  • Review protocols and study documents as required.
  • Train and demonstrate competency in independent central radiology review.
  • Assist in oversight of central reader assignments and training.
  • Participate in variability assessments and sponsor visits/audits.
  • Collaborate with management to resolve technical concerns.
  • Contribute to SOPs and study procedures.
  • Perform other duties as assigned.

Connaissances

MD with licensure
Radiology imaging expertise
PACS proficiency
RECIST knowledge
Board eligibility Radiology

Formation

Medical Doctor (MD) degree

Outils

PACS

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.

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