Bengaluru Karnataka Entry level clinical research Jobs – 37 Open Jobs Today

Clinical Data Coordinator II
Quanticate —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Oracle
- Health insurance
- Paid time off
Quick apply
Clinical Data Associate II
Precision for Medicine —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Pharmacovigilance Services Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Drug Safety Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Nursing
- B.Sc
- Bachelor's degree
Pharmacovigilance Services Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
14d
Clinical Data Associate II
Precision Medicine Group —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Data Management Assistant II
Labcorp —Bengaluru, Karnataka
- Full-time
- Microsoft Excel
- Laboratory experience
- Research
2d
Data Management Asst II
Labcorp —Bengaluru, Karnataka
- Full-time
- Microsoft Excel
- Laboratory experience
- Research
2d
Senior Drug Safety Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Drug Safety Scientist
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
14d
Senior Clinical Data Associate
Precision Medicine Group —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
3d
Senior Drug Safety Scientist
Accenture —Bengaluru, Karnataka
- Full-time
- Medicine
- Bachelor's degree
- Data entry
Project Technical Support III- ICMR FIW-TB TDM study Project
St. John’s National Academy of Health Sciences —Bengaluru, Karnataka
- ₹36,400 a month
- Email
- Nursing
- B.Sc
- Laboratory experience
14d
Pharmacovigilance Services Specialist
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Senior Clinical Data Associate
Precision for Medicine —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
3d
Pharmacovigilance Services Sr Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Bachelor's degree
- Data entry
Sr Eng, Systems
Baxter —Bengaluru, Karnataka
- English
- Research
- Electrical experience
- Paid time off
Eng II, Electrical
Baxter —Bengaluru, Karnataka
- English
- Research
- Bachelor's degree
- Paid time off
Senior Software Engineer II
Elsevier —Bengaluru, Karnataka
- Full-time
- Computer Science
- B.Sc
- Research
- Commuter assistance
- Health insurance
2d
Senior Software Engineer II
RELX —Bengaluru, Karnataka
- Full-time
- Computer Science
- B.Sc
- Research
- Commuter assistance
- Health insurance
2d

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Clinical Data Coordinator II

Quanticate -
Bengaluru, Karnataka

Quick apply

Job details

Full-time

Benefits

Health insurance
Paid time off
Flexible schedule
Paid sick time

Qualifications

Microsoft Word
Microsoft Excel
Oracle
Analysis skills
Data management
Communication skills
Time management

Full job description

At Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients.

Are you passionate about clinical research and data excellence? Do you thrive in fast-paced, dynamic environments where your attention to detail can make a real impact on patient outcomes? We’re looking for a Clinical Data Coordinator II to be at the heart of our studies, ensuring top-quality data from start to finish.

What You’ll Do

Support end-to-end Clinical Data Management activities across multiple studies
Assist with database testing and validation prior to study activation
Prepare and maintain study-specific Data Management documentation
Review CRFs critically, identifying data inconsistencies, errors, or missing information
Raise, track, and resolve data queries and Data Clarification Forms (DCFs)
Manage self-evident queries and allowable data changes within the database
Perform quality control checks on data entry and database outputs
Support study close-out activities, including preparation of archival documentation
Ensure compliance with SOPs, ICH-GCP, regulatory requirements, and client standards
Contribute to process improvement initiatives and data management best practices
Perform medical coding activities when assigned
Collaborate with offshore data processing and programming teams
Provide project updates and support progress tracking using reports and metrics
Take on ad-hoc tasks as required to support project and team objectives

What You’ll Gain

Exposure to full lifecycle Clinical Data Management across diverse studies
Hands-on experience working with industry-leading CDM systems
Opportunity to collaborate with cross-functional and global teams
Development of leadership, coordination, and project oversight skills
A supportive environment that values quality, compliance, and continuous improvement
Career growth within a regulated and evolving clinical research setting

Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs.

Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development

We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.

Requirements

Knowledge:

Strong understanding of Clinical Data Management processes
Solid knowledge of ICH-GCP guidelines and regulatory requirements related to data handling
Familiarity with CRO and sponsor-driven study standards

Work Experience:

Prior experience in Clinical Data Management or a similar role
Hands-on experience with at least one CDM system (e.g., Oracle Clinical, Medidata Rave, Inform)
Experience supporting multiple studies or managing competing priorities is preferred

Skills:

Excellent attention to detail and strong analytical thinking
Good written and verbal communication skills
Strong organizational and time-management abilities
Ability to work effectively in a fast-changing, deadline-driven environment
Comfortable working with offshore or remote teams
Proficient in Microsoft Word and Excel
Team-oriented mindset with the ability to motivate and collaborate effectively

Quanticate will never ask for payments as part of the recruitment or hiring process, and all legitimate correspondence from Quanticate will come exclusively from our @quanticate.com domain name. Hiring at Quanticate is based purely on merit and we do not ask or require candidates to deposit any money or complete any paid for courses as part of the process. Further guidance on our recruitment process and tips on how to stay safe during your job search can be found on our website at https://www.quanticate.com/careers-guidance.

Benefits

Competitive salary
Flexible working hours
Holidays (Annual Leave, Sick Leave, Casual Leave and Bank holidays)
Medical Insurance for self and immediate family
Gratuity
Accidental Coverage
Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e- learning, job shadowing)

Quick apply

Refine Your Search

entry level clinical research jobs in bengaluru karnataka

Clinical Data Coordinator II

Clinical Data Associate II

Pharmacovigilance Services Analyst

Drug Safety Associate

Pharmacovigilance Services Associate

Clinical Data Associate II

Data Management Assistant II

Data Management Asst II

Senior Drug Safety Associate

Drug Safety Scientist

Senior Clinical Data Associate

Senior Drug Safety Scientist

Project Technical Support III- ICMR FIW-TB TDM study Project

Pharmacovigilance Services Specialist

Senior Clinical Data Associate

Pharmacovigilance Services Sr Analyst

Sr Eng, Systems

Eng II, Electrical

Senior Software Engineer II

Senior Software Engineer II

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