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    • Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
    • Review diagnostic reports and validate that the correct category and subcategory are selected (e.g., CT-Abdomen, Ultrasound-Transvaginal).
    • Candidates should be Degree/Diploma in Bio Medical with minimum of 2 to 3 years experience preferably in Hospital.
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    • It's a field job.*.
    • Job Types: Full-time, Permanent, Fresher.
    • Prepare execution plans outlining timelines for medical equipment.
    • Provide training to end users on installed medical equipment.
    • The role is suitable for fresh graduates as well as experienced medical sales professionals who want to build long-term careers in pharmaceutical and healthcare…
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    • Answering questions: Providing advice and answering queries from healthcare professionals.
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    • Participate in medical conferences, trade shows, and other industry events relevant to Anantnag.
    • Jupiven Pharmaceuticals Pvt. Ltd.* is seeking an enthusiastic…
    • Coordinate regulatory activities and support ongoing medical device projects.
    • We are seeking a Regulatory Coordinator with prior *Johnson & Johnson / DePuy…
    • Proven experience in transforming medical data into creative communication.
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    • Perform regular maintenance checks on medical equipment to ensure proper functionality.
    • Designs, tests, and implements medical devices and equipment;…
    • Support resolution of technical/medical doubts raised by team members.
    • 3-7 years of experience in regulatory/medical writing.
    • Quality Control (QC) of Documents.
    • Careful measurement and analytical skills.
    • A strong interest in engineering and medicine.
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    • Participate in medical conferences, trade shows, and other industry events relevant to Jammu.
    • Jupiven Pharmaceuticals Pvt. Ltd.* is seeking an enthusiastic and…

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Job Post Details

Clinical Research Associate - job post

KLINSCIENCE HEALTHCARE
Pune, Maharashtra
₹2,75,000 - ₹3,30,000 a year

Job details

Pay

  • ₹2,75,000 - ₹3,30,000 a year

Job type

  • Permanent
  • Fresher
  • Full-time

Location

Pune, Maharashtra

Benefits

Pulled from the full job description

  • Health insurance
  • Paid sick time
  • Work from home

Full job description

A CRA ensures that clinical trials are conducted ethically, safely, and in strict compliance with the study protocol and regulatory standards like Good Clinical Practice (GCP).

  • Key Responsibilities:
  • Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
  • Compliance: Ensuring the rights, safety, and well-being of trial participants are protected and that all regulatory approvals are in place.
  • Training & Liaison: Briefing site staff (doctors and coordinators) on trial procedures and acting as the primary point of contact for the sponsor.
  • Documentation: Preparing detailed monitoring reports and managing essential study files to ensure they are "audit-ready".

Job Types: Full-time, Permanent, Fresher

Pay: ₹275,000.00 - ₹330,000.00 per year

Benefits:

  • Health insurance
  • Paid sick time
  • Work from home

Work Location: In person

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