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Junior Study Start Up Submissions Coordinator

1+ years
Not Disclosed
10 June 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 Summary

Medpace, a leading global Clinical Research Organization (CRO), is hiring a Junior Study Start-Up Submissions Coordinator for its Navi Mumbai office. This full-time, on-site role offers an excellent opportunity to grow in the field of clinical research, regulatory submissions, and site activation across all trial phases. Candidates with experience in ethics submissions, ICH-GCP guidelines, and CRO operations are encouraged to apply for this exciting role in a globally recognized organization.


Key Responsibilities

  • Perform country-specific activities for activating investigative sites across clinical trial phases.

  • Prepare, review, and submit essential documents to Regulatory Agencies and Ethics Committees.

  • Collaborate with global study teams on submission progress and risk management.

  • Identify risks to site activations and propose mitigation plans.

  • Offer guidance to global teams on ethics and regulatory processes.

  • Act as the main contact for Ethical and Regulatory submission-related activities.

  • Communicate directly with investigative sites during start-up and activation phases.

  • Ensure regulatory submissions comply with applicable guidelines and regulations.

  • Advise sponsors on changing regulatory requirements.

  • Maintain accurate tracking and timely filing of submission documents.


Required Skills & Qualifications

  • Bachelor's degree in a scientific field or equivalent relevant experience.

  • Minimum 1 year of experience in a CRO, pharmaceutical company, or investigative site.

  • Proficient knowledge of ICH-GCP guidelines and regulatory frameworks.

  • Hands-on expertise in preparing and submitting regulatory documents to Ethics Committees and Regulatory Agencies.

  • Familiarity with Microsoft® Office Suite.

  • Strong organizational and communication skills.

  • Ability to formulate responses to regulatory queries.

  • Good command of written and spoken English.


Perks & Benefits

  • Competitive salary and benefits package.

  • Flexible work environment.

  • Generous paid time off (PTO) policies.

  • Structured career progression opportunities.

  • Company-sponsored employee engagement events.

  • Comprehensive health and wellness programs.


Company Description

Medpace is a scientifically-driven, full-service global Clinical Research Organization (CRO) providing Phase I-IV clinical development services to biotech, pharmaceutical, and medical device industries. With expertise across key therapeutic areas like oncology, cardiology, CNS, and infectious diseases, Medpace accelerates the development of life-changing medical therapeutics worldwide.


Work Mode

On-site (Navi Mumbai, India)


Call to Action

Ready to advance your career in clinical research? Apply now to join Medpace as a Junior Study Start-Up Submissions Coordinator and contribute to impactful global clinical trials!