Novotech Hiring Associate Clinical Data Manager

Novotech

Bengaluru

On-site

INR 800,000 - 1,200,000

Full time

14 days+
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Benefits offered by this job

Flexible work options
Hybrid work model
Inclusive policies
Wellness programs
Global exposure
Ongoing learning

Job summary

Novotech in Bangalore, India, is hiring an Associate Clinical Data Manager to oversee data management activities for assigned studies, ensure data integrity, and support global drug development projects.

The role requires 3–6 years in Clinical Data Management, familiarity with CDM tools (Medidata Rave, Oracle Clinical), knowledge of GCDMP and ICH-GCP, and strong collaboration skills. The position offers full-time, hybrid arrangements and competitive salary.

Qualifications

  • 3–6 years of experience in Clinical Data Management, preferably in CRO or pharmaceutical settings.
  • Experience with data review, database design, and query handling.
  • Familiarity with CDM tools and regulatory guidelines.

Responsibilities

  • Plan, execute, and oversee data management activities for assigned studies.
  • Review client specifications and Data Management Plans for alignment with study requirements.
  • Design, review, and validate databases, edit checks, and consistency rules.
  • Coordinate data review, cleaning, and query resolution with project teams and vendors.
  • Ensure compliance with GCDMP, ICH-GCP, and Novotech SOPs.

Skills

CDM tools
GCDMP / ICH-GCP
Communication
Teamwork
Analytical thinking

Education

Life Sciences / Pharmacy / Biotechnology degree

Tools

Medidata Rave
Oracle Clinical

Job description

Associate Clinical Data Manager Jobs | Novotech | Bangalore

Looking to advance your career in Clinical Data Management? Novotech, a leading global Contract Research Organization (CRO), is hiring experienced professionals for the role of Associate Clinical Data Manager in Bangalore, India. This is a full-time opportunity for candidates passionate about clinical trials, data integrity, and supporting groundbreaking drug development projects worldwide.

Company Overview

Novotech is a global, full-service clinical research organization (CRO) headquartered in Sydney, Australia. With over 3,000 employees and 34 offices across Asia-Pacific, North America, and Europe, Novotech is recognized for its excellence in clinical operations and regulatory expertise. The company partners with over 5,000 clinical trial sites, providing end-to-end clinical development services including data management, biostatistics, regulatory submissions, medical monitoring, and safety solutions.

Novotech’s ISO 27001 and ISO 9001 certifications demonstrate its commitment to data security, quality management, and patient safety. As an employer, Novotech fosters an inclusive workplace culture that values diversity, gender equality, and employee wellness. Employees benefit from flexible work arrangements, parental leave policies, wellness programs, and continuous professional growth opportunities.

Job Role & Responsibilities

As an Associate Clinical Data Manager, you will play a vital role in the planning, execution, and oversight of clinical data management activities for assigned studies. You will collaborate closely with project teams, clients, and external stakeholders to ensure data accuracy, consistency, and compliance with regulatory standards.

Key Responsibilities:

  • Evaluate project feasibility from a data management perspective.
  • Review client specifications, project scope, and Data Management Plans (DMPs) to ensure alignment with study requirements.
  • Design, review, and validate clinical databases, edit checks, and consistency rules.
  • Oversee and manage data review, data cleaning, and query resolution processes.
  • Perform external data reconciliation and validation of third-party data sources.
  • Operate Clinical Data Management (CDM) software for database setup, data entry, and validation.
  • Prepare, update, and maintain essential data management documentation.
  • Liaise with clinical monitoring and client teams to ensure efficient data flow and communication.
  • Coordinate with external vendors on data management deliverables.
  • Support the development of study protocols and participate in study review meetings.
  • Maintain compliance with GCDMP, ICH-GCP, and Novotech SOPs.
Eligibility / Qualifications

Education:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Biostatistics, or related disciplines.
    (Examples: B.Pharm, M.Pharm, B.Sc Biotech, M.Sc Clinical Research, B.Sc Nursing, or related fields.)

Experience:

  • 3–6 years of experience in Clinical Data Management, preferably in CRO or pharmaceutical industry settings.
  • Proven experience in data review, database design, and query handling.

Skills & Competencies:

  • Expertise in CDM tools (e.g., Medidata Rave, Oracle Clinical, or similar systems).
  • Strong understanding of GCDMP, ICH-GCP, and regulatory guidelines.
  • Excellent communication, teamwork, and analytical thinking.
  • Detail-oriented with the ability to manage multiple tasks simultaneously.
Location & Salary
  • Location: Ground Floor, Unit 1, Block E, Helios Business Park, Bangalore, 560103, India
  • Job Type: Full-time
  • Schedule: Standard working hours with flexibility as per project timelines
  • Salary: Competitive; based on qualifications and relevant experience
Work Culture & Benefits

Novotech provides a supportive, collaborative environment that encourages continuous professional development. Employees enjoy:

  • Flexible work options and hybrid models.
  • Inclusive policies for gender equality and workplace diversity.
  • Wellness and employee support programs.
  • Global exposure through cross-functional collaboration with clinical research experts worldwide.
  • Ongoing learning and upskilling through development programs.
Why Join Novotech?
  • Work with a global leader in clinical research and data management.
  • Collaborate on cutting-edge clinical trials across diverse therapeutic areas.
  • Contribute to innovations that accelerate drug development and improve patient outcomes.
  • Be part of a company recognized for its commitment to IT security and ISO-certified quality standards.
  • Thrive in a culture that values transparency, diversity, and employee well-being.
FAQs

Q1: Who can apply for the Associate Clinical Data Manager role?
Candidates with a degree in life sciences, pharmacy, or biotechnology and 3–6 years of clinical data management experience are eligible.

Q2: Is this a remote job?
This position is based in Bangalore, with flexible work options depending on project needs.

Q3: Which software tools are used in this role?
You should have experience with industry-standard CDM systems such as Medidata Rave, Oracle Clinical, or similar tools.

Q4: Does Novotech offer global exposure?
Yes. Employees collaborate with cross-functional global teams across Asia-Pacific, North America, and Europe.

Tagged as: Pharma Jobs in Bangalore

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