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Project Support Coord

0-4 years
Not Disclosed
10 Jan. 31, 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

🔍 Project Support Coordinator
📍 Location: Bengaluru, Karnataka, India
🕒 Job Type: Full-time | Onsite
🆔 Job ID: R-01217297

💡 Job Overview

As a Project Support Coordinator (PSC), you will play a vital role in supporting clinical research projects, ensuring smooth operations, compliance, and efficiency. You will be responsible for coordinating trial activities, overseeing study documentation, and providing system support for various clinical research platforms.

📌 Key Responsibilities

  • Manage & Oversee Trial Activities: Coordinate assigned trial functions, review internal and investigator files, and ensure timely resolution of issues.
  • Maintain Study Documentation & Compliance: Support study-specific documentation, oversee system access management, and track project activity plans.
  • System Support & Audit Readiness: Manage CTMS, Oracle Activate & eTMF access requests, ensure compliance, and suggest resolutions for any non-compliance issues.
  • Administrative & Operational Support: Process documents, conduct mass mailings, schedule meetings, and track study metrics.
  • Assist in Investigator Site File (ISF) Compilation: Drive the preparation of study templates, including pharmacy binders, under Clinical Team Manager guidance.
  • Project Meetings & Coordination: Attend Kickoff and Project Launch meetings, take notes, and assist in initial study setup.

🎓 Qualifications & Skills

  • Education: High school diploma or relevant academic/vocational qualification.
  • Experience: 0-4 years of experience in a similar role within clinical research or project coordination.
  • Skills Required:
    • Strong organizational and time management skills.
    • Proficiency in clinical research systems (CTMS, Oracle Activate, eTMF).
    • Ability to work independently and in a team environment.
    • Excellent attention to detail and problem-solving abilities.
    • Strong communication and coordination skills.

🌍 About Us

Our Clinical Research Services team powers the PPD® clinical research portfolio as part of a leading global Contract Research Organization (CRO). We bring scientific and clinical expertise to accelerate the development of life-changing treatments.

📌 Join us in making an impact in global healthcare! Apply now.