Data Process Associate

Quanticate

Bengaluru

On-site

INR 350,000 - 550,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Competitive salary
Six Month Intensive Training Plan
Flexible working hours
Holidays (Annual Leave, Sick Leave,Cas

Job summary

Quanticate, world leading data-focused CRO, Bengaluru, seeks a Data Process Associate to enter and verify clinical data and support data management across projects.

You will develop skills in ICH/GCP, collaborate with global teams, and grow in clinical research and data handling while contributing to healthcare outcomes.

Qualifications

  • Basic knowledge of Clinical Data Management and GCP.

Responsibilities

  • Accurately enter and verify clinical data from CRFs into study databases per guidelines.
  • Perform quality control checks to ensure data accuracy, integrity, and compliance with regulatory requirements.
  • Assist with database testing, documentation preparation, and clinical data processing across multiple projects.
  • Support User Access Management for EDC systems and maintain related documentation.
  • Collaborate with project managers and cross-functional teams to ensure timely completion of data management activities.
  • Identify process improvement opportunities and contribute to maintaining high-quality standards.
  • Perform medical coding activities and other assigned tasks to support successful study completion.

Skills

Clinical Data Management
Attention to detail
Verbal & written communication
ICH Guidelines & GCP
Excel & Word
Multi-tasking
Team collaboration
Problem solving
Quality assurance

Education

Master’s degree in Life Sciences or related field

Tools

Microsoft Excel
Microsoft Word

Job description

Step into the critical role of a Data Process Associate and contribute to the success of clinical trials by ensuring accurate and compliant data management. This role offers you the chance to develop key skills, work alongside experienced professionals, and build a strong foundation for your future in clinical research. If you're detail-focused and driven to support meaningful healthcare advancements, this is your opportunity to grow and make a difference.

What You Will Do:
  • Accurately enter and verify clinical data from Case Report Forms (CRFs) into study databases in accordance with established guidelines.
  • Perform quality control checks to ensure data accuracy, integrity, and compliance with regulatory requirements.
  • Assist with database testing, documentation preparation, and clinical data processing across multiple projects.
  • Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation.
  • Collaborate with project managers and cross-functional teams to ensure timely completion of data management activities.
  • Identify process improvement opportunities and contribute to maintaining high-quality standards.
  • Perform medical coding activities and other assigned tasks to support successful study completion.
What You Will Gain:
  • Gain hands‑on experience in clinical data management within a regulated and fast‑paced environment.
  • Develop an in‑depth understanding of industry standards, including ICH guidelines, Good Clinical Practice (GCP), and data handling regulations.
  • Gain exposure to project management and collaboration with global cross‑functional clinical research teams.
  • Strengthen analytical, communication, and technical skills using industry‑leading tools and systems.
  • Build a strong foundation for career growth in clinical research and data management.
  • Contribute to clinical studies that help advance healthcare and improve 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 carewyou want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter.

Education
  • Master’s degree in Life Sciences or a related field.
Skills & Knowledge
  • Basic knowledge of Clinical Data Management.
  • Strong analytical skills with excellent attention to detail.
  • Good verbal and written communication skills.
  • Basic knowledge of ICH Guidelines and Good Clinical Practice (GCP), including regulatory requirements related to clinical development programs, data handling, and data processing.
  • Proficiency in PC applications, including Microsoft Excel and Word.
  • Ability to manage multiple competing priorities in a dynamic and fast‑changing environment.
  • Ability to work effectively within teams, inspire collaboration, and motivate colleagues to achieve project goals.
  • Strong organizational and problem‑solving skills
  • Ability to maintain accuracy and quality while working under deadlines.

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

  • Competitive salary
  • Six Month Intensive Training Plan
  • 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)
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Clinical Data Coordinator II India Data Management
Clinical Data Coordinator II India Data Management

Quanticate International Limited • Bengaluru

On-site
INR 600,000 - 900,000
Competitive salary
Flexible working hours
Holidays including annual and sick leave
+4
Document Specialist (Consultant)
Document Specialist (Consultant)

Quanticate • India

On-site
INR 900,000 - 1,500,000
Competitive salary
Flexible working hours
Holidays (Annual Leave, Sick Leave,Cas
+4
Team Lead of Biometrics Automation & AI Architecture
Team Lead of Biometrics Automation & AI Architecture

Quanticate • Bengaluru

On-site
INR 350,000 - 520,000
Competitive salary
Flexible hours
Annual leave
+4
Senior Programmer III
Senior Programmer III

Quanticate • Bengaluru

On-site
INR 600,000 - 1,000,000
Competitive salary
Flexible working hours
Medical Insurance
+2
Senior Clinical Data Associate Bangalore, Karnataka, India
Senior Clinical Data Associate Bangalore, Karnataka, India

Precision Medicine Group • Bengaluru

On-site
INR 900,000 - 1,300,000
Senior Clinical Data Associate Bangalore, Karnataka, India
Senior Clinical Data Associate Bangalore, Karnataka, India

Precision Medicine Group • Bengaluru

On-site
INR 900,000 - 1,200,000
Medical Writer
Medical Writer

Quanticate • Bengaluru

On-site
INR 1,500,000 - 2,500,000
Competitive salary
Flexible hours
Holidays
+4
Clinical Data Manager
Clinical Data Manager

Avance Clinical Pty Ltd. • Bengaluru

On-site
INR 900,000 - 1,300,000
Stimulating work
Project diversity
Career progression
+2
Senior Clinical Data Associate
Senior Clinical Data Associate

Precision Medicine Group • Chennai District

On-site
INR 1,200,000 - 2,400,000
Clinical Data Specalist / Senior clinical Data Coordinator
Clinical Data Specalist / Senior clinical Data Coordinator

IQVIA • Ernakulam

On-site
INR 600,000 - 800,000