H .s .r Layout B .d .a Complex Karnataka Pharmaceutical industry Jobs – 569 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
Pharmacovigilance Services New Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Bachelor's degree
- Data entry
Pharmacovigilance Services Associate
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
Pharmacovigilance Services Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Analysis skills
- Bachelor's degree
- Data entry
Customer Service Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- 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 Specialist
Accenture —Bengaluru, Karnataka
- Full-time
- Medicine
- Bachelor's degree
- Data entry
Quality Specialist (QMS, Documentation)
Merck KGaA —Bengaluru, Karnataka
- Master's degree
- Communication skills
Regulatory Analyst - Clinical Affairs
Remidio —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
- Time management
Job Description - Research Assistant – InVitro
Quantumzyme —Bengaluru, Karnataka
- Laboratory experience
- Research
- Master's degree
Pharmacovigilance Services Sr Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
ING03-301268 Orc-SC and CRM-NF-GDS-NS
EY —Bengaluru, Karnataka
- Microsoft Excel
- Master's degree
- Analysis skills
Clinical Trial Implementation Specialist
DSG Inc —Hoodi, Bengaluru, Karnataka
- Call employer
- Health insurance
- Paid time off
Life Sciences (Pharmaceutical) Research Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Doctoral degree
Medical Representative (MR)
Cadila Pharmaceuticals —Bangalore City, Bengaluru, Karnataka
- Full-time
- Sales
- B.Sc
- Bachelor's degree
- Health insurance
- Life insurance
Quick apply
Medical Writer
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- Writing skills
- English
6d
Medical Representative
Cadila Pharmaceuticals —Bangalore City, Bengaluru, Karnataka
- Full-time
- B.Sc
- Bachelor's degree
- Travel
- Health insurance
- Paid sick time
Quick apply
5d
Project Coordinator
Endpoint Clinical —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Microsoft Excel
- Customer service
- Microsoft Office
1d
Clinical Data Manager
DSG Inc —Hoodi, Bengaluru, Karnataka
- Customer service
- Bachelor's degree
- Organisational skills
R&D Associate - Organic Chemistry
Atomgrid —Bengaluru, Karnataka
- ₹4,00,000 - ₹6,00,000 a year
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
- Health insurance
- Paid time off
Quick apply

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Clinical Data Coordinator I

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
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

pharmaceutical industry jobs in h .s .r layout b .d .a complex karnataka

Clinical Data Coordinator I

Pharmacovigilance Services New Associate

Pharmacovigilance Services Associate

Pharmacovigilance Services Analyst

Customer Service Analyst

Clinical Data Coordinator II

Pharmacovigilance Services Specialist

Quality Specialist (QMS, Documentation)

Regulatory Analyst - Clinical Affairs

Job Description - Research Assistant – InVitro

Pharmacovigilance Services Sr Analyst

ING03-301268 Orc-SC and CRM-NF-GDS-NS

Clinical Trial Implementation Specialist

Life Sciences (Pharmaceutical) Research Associate Manager

Medical Representative (MR)

Medical Writer

Medical Representative

Project Coordinator

Clinical Data Manager

R&D Associate - Organic Chemistry

I want to receive the latest job alerts for pharmaceutical industry in h .s .r layout b .d .a complex karnataka

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