Radiologist Medpace | Corporate Navi Mumbai

Medpace is a full-service global Clinical Research Organisation (CRO) providing Phase I–IV clinical development services. Headquartered in Cincinnati, Ohio, Medpace employs over 6,000 professionals across more than 40 countries, with expertise spanning oncology, cardiology, endocrinology, neuroscience, metabolic diseases, and infectious diseases.

Medpace seeks an experienced Radiologist – Core Laboratory to join its office‑based team in Navi Mumbai. This full‑time position focuses on interpreting imaging studies for clinical trials, collaborating with multidisciplinary teams, ensuring compliance with Good Clinical Practice (GCP) guidelines, and supporting global research programs.

• Job Title:
  
  Radiologist – Core Laboratory
• Req
• Location:
  
  Navi Mumbai, India
• Department:
  Physicians & Medical Directors
• Employment Type:
  
  Full Time
• Job Category:
  Clinical Research

• Interpret radiology examinations according to standard medical practice, study protocols, GCP guidelines, and Medpace SOPs.
• Complete source documents accurately and within required timelines.
• Review clinical study protocols, imaging charters, and technical documentation.
• Participate in Inter Reader and Inter Reader variability assessments.
• Demonstrate competency in operating radiology research equipment.
• Support sponsor site visits and regulatory audits when required.
• Collaborate with management to resolve technical, radiological, and study‑related issues.
• Participate in the development, review, and evaluation of Standard Operating Procedures (SOPs).
• Perform additional responsibilities assigned by the organisation.

• M.D. (Doctor of Medicine)
• Current medical licensure
• Board eligibility in Radiology or equivalent training demonstrating competency

• Experience with multi‑modality imaging projects
• Experience using medical imaging software
• Knowledge of RECIST 1.1 response criteria
• Proficiency in Microsoft Word, Excel, Access, and Project

• Diagnostic radiology expertise
• Clinical research knowledge
• Medical imaging interpretation
• Good Clinical Practice (GCP) compliance
• Multi‑modality imaging experience
• Imaging software proficiency
• Clinical trial documentation
• Strong analytical and reporting skills
• Attention to detail
• Cross‑functional collaboration
• Problem‑solving abilities
• Excellent communication skills
• Knowledge of RECIST 1.1
• Ability to participate in sponsor audits and inspections