Yelahanka New Town Bengaluru Karnataka Research associate Jobs – 860 Open Jobs Today

Clinical Research Associate
TrialGuna Pvt Ltd —Bengaluru, Karnataka
- ₹5,00,000 - ₹6,00,000 a year
- Full-time
- Research
- Bachelor's degree
- In-person
- Paid time off
- Cell phone reimbursement
Quick apply
10d
Research Associate
TERI —Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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Research Associate I
Vantive —Bengaluru, Karnataka
- Research
- Analysis skills
Research Associate
Scinva Chemicals and Pharmaceuticals Pvt Ltd —Bengaluru, Karnataka
- Full-time
- Computer literacy
- B.Sc
- Master's degree
Quick apply
Research Associate - Fragrances & Flavors
ITC Limited —Bengaluru, Karnataka
- Full-time
- Master's degree
- Communication skills
Research Associate
Pan Seeds —Bengaluru, Karnataka
- Microsoft Powerpoint
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Junior Research Associate - Consumer And Sensory Sciences
ITC Limited —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
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Clinical Research Associate I
PSI CRO —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Travel
Quick apply
8d
Research Associate - SparX
Meraki-Labs —Bengaluru, Karnataka
- Full-time
- English
- Research
- Master's degree
Quick apply
7d
Research Associate
ITC Limited —Bengaluru, Karnataka
- Full-time
- Master's degree
- Computer skills
- Communication skills
Associate Consultant
Weaver and Tidwell India LLP —Indira Nagar, Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Excel
- English
Associate - Market Research and Insights
Deloitte —Bengaluru, Karnataka
- English
- Research
- Microsoft Office
Strategy and Operations Associate
Turing —Bengaluru, Karnataka
- Microsoft Excel
- Engineering
- Project management
- Flexible schedule
IN-Associate–KYC&AML --FinCrime Coe- Advisory– Bangalore
PwC —Bengaluru, Karnataka
- Full-time
- Analysis skills
- Bachelor's degree
- Travel
Survey Research Project Coordinator
Gallup —Bengaluru, Karnataka
- Hybrid work
- Microsoft Powerpoint
- Research
- Master's degree
- Health insurance
- Life insurance
Research Associate - THAAI Study Project
St. John’s National Academy of Health Sciences —Bengaluru, Karnataka
- ₹30,000 a month
- Email
- English
- Master's degree
- Data entry
Business Development Associate
Tatvaops —HSR Layout, Bengaluru, Karnataka
- From ₹5,00,000 a year
- Full-time
- CRM software
- Microsoft Excel
- English
- Cell phone reimbursement
- Food provided
Quick apply
Project Associate
Newspace —Bengaluru, Karnataka
- Research
- Microsoft Office
- Administrative experience
Quick apply
Research Associate - Consumer & Sensory Sciences
ITC Limited —Bengaluru, Karnataka
- Full-time
- Research
- Master's degree
- Communication skills
Analyst Customer Alert/Enhanced Due Diligence
Empower Annuity Insurance Company of America —Bengaluru, Karnataka
- Microsoft Excel
- Microsoft Outlook
- Research
2d

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Clinical Research Associate

TrialGuna Pvt Ltd
Bengaluru, Karnataka

Quick apply

Job details

Full-time
₹5,00,000 - ₹6,00,000 a year
10 days ago

Benefits

Provident Fund
Paid time off
Cell phone reimbursement

Qualifications

Clinical research
Research
Bachelor's degree
Data collection
Medical terminology

Full job description

Job Title: Clinical Research Associate

Department: Clinical Operations

Location: Bengaluru, Karnataka Reports To: Sr Project Manager

Job Summary

The Clinical Research Associate (CRA) ensures the smooth execution of clinical trials by managing compliance, site coordination, data management, and ethical oversight. This role involves collaborating with investigators, sponsors, and regulatory bodies to maintain protocol adherence, patient safety, and GCP compliance while overseeing study logistics and documentation.

Key Responsibilities1. Regulatory Compliance:

· Ensure compliance with general and study specific regulatory requirements

· Conduct study activities in alignment with local, federal, and state regulations and institutional policies.

· Submission of EC Dossier and coordination with IEC/IRB to get approvals for the Clinical Trial Conduct.

2. Site Management:

· Coordinate and execute site selection, initiation and close-out visits.

· Conduct training for site staff on trial-specific industry standards and procedure.

3. Study Coordination:

· Facilitate daily clinical trial activities, including scheduling study subject appointments and serving as a liaison between patients, principal investigators (PIs) and other study personnel.

· Support the informed consent process by clearly communicating study protocols and answering questions from potential subjects.

4. Participant Management & Communication:

· Facilitate clear and effective communication with CROs, sponsors, investigators, research teams, laboratories, and vendors.

· Serve as the primary contact for study-related inquiries from sponsors, and regulatory authorities.

5. Data Management:

· Maintain and manage study records, including Case Report Forms (CRFs), Drug Dispensation Records and Regulatory Forms.

6. Communication:

· Serve as the primary contact for study sites, CROs, sponsors, Vendors, ensuring timely communication and support.

7. Ethics and Oversight:

· Coordinate with ethics committees to ensure the rights and welfare of study participants are safeguarded.

· Report any suspicion of research misconduct to promote ethical research conduct.

8. Documentation and Reporting:

· Review the data collated by the CRC and ensure completeness and accuracy.

· Aid in archival of study documentation.

· Write visit reports and maintain comprehensive records of trial related activities.

9. Protocol Development:

· Assist in the development of trial protocols, including methodology and data collection forms (CRFs)

10. Inventory and IP Management:

· Oversee investigational product (IP) management, including receipt, storage, dispensation, and accountability.

· Manage investigational product (IP) supplies, ensuring all materials are accounted for and properly distributed to trial sites.

· Coordinate the close-down of trial sites upon completion of the study.

Secondary Responsibilities:

1. Ensuring Compliance with SOP’s, Legal Regulations, ICH and GCP guidelines

2. Overall Responsibilities: Protocol Compliance, GCP compliance, GDP compliance, SOP compliance.

Pay: ₹500,000.00 - ₹600,000.00 per year

Benefits:

Cell phone reimbursement
Paid time off
Provident Fund

Work Location: In person

Quick apply

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