Bio Medical jobs
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- KLINSCIENCE HEALTHCAREPune, Maharashtra
- Health insurance
- Paid sick time
- Work from home
- Site Monitoring: Conducting on-site or remote visits to verify that trial data matches original medical records (Source Data Verification).
- View all KLINSCIENCE HEALTHCARE jobs - Pune, Maharashtra jobs
- Salary Search: Clinical Research Associate salaries in Pune, Maharashtra
- DemandPayBengaluru, Karnataka
- Health insurance
- Leave encashment
- Provident Fund
- Review diagnostic reports and validate that the correct category and subcategory are selected (e.g., CT-Abdomen, Ultrasound-Transvaginal).
- Holy Family HospitalDelhi
- Candidates should be Degree/Diploma in Bio Medical with minimum of 2 to 3 years experience preferably in Hospital.
View similar jobs with this employerCadila PharmaceuticalsKochi, Kerala- Paid sick time
- Provident Fund
- Flexible schedule
- It's a field job.*.
- Job Types: Full-time, Permanent, Fresher.
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- See popular questions & answers about Cadila Pharmaceuticals
- Shubham EPCMumbai, Maharashtra
- Prepare execution plans outlining timelines for medical equipment.
- Provide training to end users on installed medical equipment.
Medical Representative
Often replies in 4 daysBioincro India LLPDelhi, Delhi- Commuter assistance
- 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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View similar jobs with this employerAdven biotechSrinagar, Jammu and Kashmir- Answering questions: Providing advice and answering queries from healthcare professionals.
- Influencing prescriptions: Using their knowledge of products and…
- jupiven pharmaceuticals pvt ltdAnantnag, Jammu and Kashmir
- Health insurance
- Provident Fund
- Flexible schedule
- Participate in medical conferences, trade shows, and other industry events relevant to Anantnag.
- Jupiven Pharmaceuticals Pvt. Ltd.* is seeking an enthusiastic…
- DEV-XRemote
- Coordinate regulatory activities and support ongoing medical device projects.
- We are seeking a Regulatory Coordinator with prior *Johnson & Johnson / DePuy…
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- UNISTAR BIOTECH LTDBhagalpur District, Bihar
- Minimum 1 years experience in same HQ.
- Total work: 1 year (Preferred).
- Medisage E-Learning Pvt. Ltd.Mumbai, Maharashtra
- Health insurance
- Cell phone reimbursement
- Provident Fund
- Proven experience in transforming medical data into creative communication.
- Provide medical perspective to creative and strategy teams to strengthen…
- VitaLifePune, Maharashtra
- Perform regular maintenance checks on medical equipment to ensure proper functionality.
- Designs, tests, and implements medical devices and equipment;…
- VitaLifePune, Maharashtra
- Perform regular maintenance checks on medical equipment to ensure proper functionality.
- Designs, tests, and implements medical devices and equipment;…
- GoStravvyGurugram, Haryana
- Food provided
- Health insurance
- Paid time off
- Paid sick time
- Provident Fund
- Support resolution of technical/medical doubts raised by team members.
- 3-7 years of experience in regulatory/medical writing.
- Quality Control (QC) of Documents.
- iKing Tech SolutionsVellore, Tamil Nadu
- Careful measurement and analytical skills.
- A strong interest in engineering and medicine.
- Install, adjust, maintain, repair, or provide technical support for…
- jupiven pharmaceuticals pvt ltdJammu, Jammu and Kashmir
- Health insurance
- Provident Fund
- Flexible schedule
- Participate in medical conferences, trade shows, and other industry events relevant to Jammu.
- Jupiven Pharmaceuticals Pvt. Ltd.* is seeking an enthusiastic and…
Job Post Details
Clinical Research Associate - job post
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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