Bengaluru, Karnataka Clinical research Jobs – 493 Open Jobs Today

Clinical Data Coordinator I
Quanticate —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Oracle
- Health insurance
- Paid time off
Quick apply
1d
Initiation Clinical Research Associate I
Parexel —Bengaluru, Karnataka
- Analysis skills
- Data entry
- Computer skills
Pharmacovigilance Services New Associate
Accenture —Bengaluru, Karnataka
- Full-time
- B.Sc
- Bachelor's degree
- Data entry
Pharmacovigilance Services Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Analysis skills
- Bachelor's degree
- Data entry
Clinical Data Coordinator II
Quanticate —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Oracle
- Health insurance
- Paid time off
Quick apply
Pharmacovigilance Services Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Pharmacovigilance Services Specialist
Accenture —Bengaluru, Karnataka
- Full-time
- Medicine
- Bachelor's degree
- Data entry
Clinical Data Coordinator 2
Veranex, Inc. —Bengaluru, Karnataka
- Word processing
- Databases
- Bachelor's degree
Quick apply
3d
Clinical Research Associate II
Fortrea —Bengaluru, Karnataka
- Full-time
- Patient monitoring
- Customer service
- Computer literacy
School / College Counselor (M.Sc Counselling/Clinical/Forensic Psychology)
Cadabams Group —JP Nagar, Bengaluru, Karnataka
- ₹20,000 - ₹30,000 a month
- Email
- English
- Master's degree
- In-person
- Health insurance
- Paid time off
Quick apply
Research and Psychometric Services Assistant(Advanced Associate, Scoring Service)
Pearson —Bengaluru, Karnataka
- Full-time
- English
- Master's degree
- Psychology
Senior Clinical Research Associate
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
Coordinator Support I
Labcorp —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
10d
Clinical Research Scientist
Niramai —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Computer networking
Clinical Research Associate / Senior CRA
Remidio —Bengaluru, Karnataka
- Python
Pharmacovigilance Services Sr Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Clinical Data Svs Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
Clinical Data Associate II
Precision Medicine Group —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Medical/Scientific Editor
M3EU —Bengaluru, Karnataka
- Full-time
- Remote
- Communication skills
- Marketing
Quick apply
Life Sciences (Pharmaceutical) Research Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Doctoral degree

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Clinical Data Coordinator I

Quanticate -
Bengaluru, Karnataka

Quick apply

Job details

Full-time
1 day ago

Benefits

Health insurance
Paid time off
Flexible schedule
Paid sick time

Qualifications

Microsoft Word
Microsoft Excel
Oracle
Analysis skills
Bachelor's degree
Data management
Data entry
Project leadership
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 database testing: Help validate study databases before activation.
Prepare documentation: Assist in creating study-specific materials.
Process clinical data: Ensure accuracy and completeness of project data.
Review CRFs: Critically check Case Report Forms against the Data Management Plan and raise queries when needed.
Resolve queries: Track and resolve Data Clarification Forms, self-evident queries, and allowable changes.
Perform quality control: Conduct QC checks on data entry and CRFs/databases.
Manage archiving: Prepare documentation for client return or internal archiving at study completion.
Contribute to improvements: Suggest enhancements to processes and standards.
Medical coding: Perform coding activities when assigned.
Collaborate with teams: Work with project managers, sponsors, investigators, and offshore teams to ensure smooth delivery.

What You’ll Gain

Hands-on experience: Exposure to end-to-end clinical data management across multiple studies.
Skill development: Strengthen expertise in database testing, CRF review, query resolution, and medical coding.
Quality mindset: Learn to work to industry standards, SOPs, and regulatory guidelines.
Career growth: Build a foundation for advancement in clinical data management and project leadership.
Collaboration opportunities: Gain experience working with global teams and diverse stakeholders.
Contribution to healthcare: Play a vital role in ensuring reliable data that supports medical research and patient outcomes.

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

clinical research jobs in bengaluru, karnataka

Clinical Data Coordinator I

Initiation Clinical Research Associate I

Pharmacovigilance Services New Associate

Pharmacovigilance Services Analyst

Clinical Data Coordinator II

Pharmacovigilance Services Associate

Pharmacovigilance Services Specialist

Clinical Data Coordinator 2

Clinical Research Associate II

School / College Counselor (M.Sc Counselling/Clinical/Forensic Psychology)

Research and Psychometric Services Assistant(Advanced Associate, Scoring Service)

Senior Clinical Research Associate

Coordinator Support I

Clinical Research Scientist

Clinical Research Associate / Senior CRA

Pharmacovigilance Services Sr Analyst

Clinical Data Svs Associate

Clinical Data Associate II

Medical/Scientific Editor

Life Sciences (Pharmaceutical) Research Associate Manager

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