Bengaluru Karnataka Associate clinical operations Jobs – 66 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
8d
Drug Safety Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Nursing
- B.Sc
- Bachelor's degree
Consulting Associate
Huron Eurasia India Private Limited —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Manager, Clinical Operations
Parexel —Bengaluru, Karnataka
- Public speaking
- English
- Travel
7d
Associate Analyst
Eurofins GSC IT DC —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
13d
Associate Clinical Data Programmer
Novo Nordisk —Bengaluru, Karnataka
- Azure
- B.Sc
- English
Associate, OM
Bruker —Bengaluru, Karnataka
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sr. Clinical Research Associate
Emmes Group —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Office
- Bachelor's degree
- Organisational skills
5d
Associate Functional Programmer
Novo Nordisk —Bengaluru, Karnataka
- Computer Science
- English
- Master's degree
2d
LifeScience Regulatory Svs Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
HR Associate
Dezy —Bengaluru, Karnataka
- Bachelor's degree
- Human resources
- Computer networking
Quick apply
Health Admin Services Associate-Voice
Accenture —Bengaluru, Karnataka
- Full-time
- Nursing
- B.Sc
- English
- Health insurance
Associate Director, Clinical Data Scientist
Takeda Pharmaceutical —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- SQL
- Machine learning
- Health insurance
- Cell phone reimbursement
Senior Drug Safety Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Quality Assurance Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- B.Sc
- Bachelor's degree
Health Admin Services New Associate-Voice
Accenture —Bengaluru, Karnataka
- Full-time
- Nursing
- B.Sc
- English
- Health insurance
India GGC - Client Account Management
Accenture —Bengaluru, Karnataka
- Full-time
- ERP systems
- Master's degree
- Business development
Lead, Clinical Data Processor
Clario —Bengaluru, Karnataka
- Full-time
- Microsoft Word
- Microsoft Excel
- Computer Science
- Health insurance
Associate Director, Computational Biology
Takeda Pharmaceutical —Bengaluru, Karnataka
- Full-time
- Management
- Doctoral degree
- Research
HR Associate
smiles.ai —Bengaluru, Karnataka
- Bachelor's degree
- Human resources
- Computer networking

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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
8 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

Refine Your Search

associate clinical operations jobs in bengaluru karnataka

Clinical Research Associate

Drug Safety Associate

Consulting Associate

Manager, Clinical Operations

Associate Analyst

Associate Clinical Data Programmer

Associate, OM

Sr. Clinical Research Associate

Associate Functional Programmer

LifeScience Regulatory Svs Associate

HR Associate

Health Admin Services Associate-Voice

Associate Director, Clinical Data Scientist

Senior Drug Safety Associate

Quality Assurance Associate Manager

Health Admin Services New Associate-Voice

India GGC - Client Account Management

Lead, Clinical Data Processor

Associate Director, Computational Biology

HR Associate

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