Novotech Hiring Associate Clinical Data Manager
- Associate Clinical Data Manager Jobs | Novotech | Bangalore
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Work Culture & Benefits
- Application Process
- Why Join Novotech?
- FAQs
- Vertical Summary Table
Associate Clinical Data Manager Jobs | Novotech | Bangalore
Apply for Associate Clinical Data Manager jobs at Novotech, Bangalore. Life science graduates with 3–6 years of experience preferred.
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.
Application Process
Interested candidates can apply directly via Novotech’s official career portal:
Apply Now
Don’t miss this opportunity — apply early to secure your position as an Associate Clinical Data Manager at one of the world’s fastest-growing CROs!
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.
Q5: How can I apply?
Visit the official Novotech career page and submit your application.
Vertical Summary Table
| Company | Novotech (Global CRO) |
|---|---|
| Vacancies | Associate Clinical Data Manager |
| Required Education | Bachelor’s/Master’s in Life Sciences, Pharmacy, Biotechnology, Clinical Research |
| Experience | 3–6 years in Clinical Data Management |
To apply for this job please visit fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com.
