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Eclinical Coordinator

1-2 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: eClinical Coordinator
Location: Navi Mumbai, India
Department: Data Management
Job ID: 10890

Job Summary:

Medpace is seeking a full-time, office-based eClinical Coordinator to join our Data Management / eClinical team in Navi Mumbai, India. As an eClinical Coordinator, you will work closely with the eClinical Project Manager and other team members to ensure the accuracy of the data reported by patients for clinical studies. This role is ideal for detail-oriented individuals who enjoy a predictable and standardized work environment. We provide an extensive onboarding and training process to prepare you to become an expert in the field.

Responsibilities:

  • System Design & Setup: Assist the Project Manager in system design and setup.
  • Study Documentation: Create study-specific documents for clinical trials.
  • Project Monitoring: Track and provide key study metrics, ensuring proper monitoring of the project.
  • Client Interaction: Work with clients to obtain requirements and respond to their inquiries.
  • Additional Tasks: Support with other assigned projects and tasks as needed.

Qualifications:

  • Education: Bachelor’s degree in a health-related field with strong attention to detail.
  • Skills:
    • Proficient in Excel and Word.
    • Knowledge of medical terminology.
  • Experience:
    • 1-2 years of experience in a pharmaceutical or CRO setting preferred.

Travel: None

Medpace Overview:

Medpace is a full-service clinical contract research organization (CRO) offering Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the development of safe and effective therapeutics globally, leveraging local regulatory and therapeutic expertise across areas including oncology, cardiology, metabolic diseases, endocrinology, CNS, anti-viral, and anti-infective.

Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.

Why Medpace?

  • People. Purpose. Passion: Contribute to improving global healthcare.
  • Perks:
    • Competitive compensation and benefits
    • Employee wellness initiatives
    • Structured career paths for professional growth
    • Employee appreciation events
    • Flexible work environment (position dependent)

If you're interested in contributing to the success of clinical trials and want to be part of a dynamic team, apply now and join Medpace!