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Associate Clinical Data Manager – Novotech Careers India
Novotech, a leading global full-service clinical Contract Research Organization (CRO), is hiring an Associate Clinical Data Manager in India. This position is ideal for professionals with experience in clinical data management who are passionate about contributing to global clinical research. The Clinical Data Manager role involves overseeing data management activities, ensuring accuracy and compliance with clinical and regulatory standards, and collaborating with global teams on innovative life science projects at Novotech Careers.
Clinical Data Manager Job Details:
- Job Title: Associate Clinical Data Manager
- Location: India
- Department: Biometrics
- Reporting To: Biometrics Project Manager
- Employment Type: Full-Time
- Experience Required: 3–6 years in Clinical Data Management or related roles
- Industry: Pharmaceutical / Clinical Research / CRO
Clinical Data Manager Role Overview:
The Associate Clinical Data Manager is responsible for planning, executing, and managing all aspects of clinical data management for assigned trials. The role includes feasibility assessment, database design, validation, data cleaning, and ensuring data accuracy in compliance with Good Clinical Data Management Practices (GCDMP) and regulatory guidelines.
About the Company:
Novotech is a global, full-service clinical Contract Research Organization (CRO) headquartered in Sydney, Australia. With 34 offices across Asia-Pacific, North America, and Europe, Novotech employs over 3,000 professionals and partners with more than 5,000 clinical sites.
The company offers comprehensive clinical development services across all trial phases and therapeutic areas, including regulatory submissions, data management, biostatistics, medical monitoring, and safety management. Novotech is ISO 27001 and ISO 9001 certified, ensuring world-class quality and information security standards.
At Novotech, employees work within a collaborative, inclusive culture that values innovation, empowerment, and professional growth. The organization is committed to equality, flexibility, and wellness for its global workforce.
Responsibilities for the Clinical Data Manager Role:
- In these Clinical Data Management Jobs, you should have determination of project feasibility from a data management perspective. Understand the requirements of the project agreement and scope to ensure that Novotech performs these services as required.
- Perform comprehensive data management tasks including data review, query management, external data reconciliation.
- Design and review of database structure, validation rules and consistency checks.
- Operation of Clinical Data Management software for data entry of clinical trial results.
- All data cleaning/validation tasks.
- Development of all key Data Management Documents.
- Liaison with client companies / monitoring staff as appropriate, ensuring effective study communication with internal and external stakeholders.
- Liaison with external service providers on Data Management projects as appropriate.
- Assist in the development of protocols as required.
Experience and Qualifications:
- Graduate in a clinical or life sciences related field.
- At least three to six years experience working in a Clinical Data Associate (or equivalent) role in a Pharmaceutical industry or related role.
Skills Required:
- These Clinical Data Management Jobs, require strong analytical and organizational skills.
- Proficiency in clinical data management tools and EDC systems.
- Excellent attention to detail and data accuracy.
- Strong written and verbal communication abilities.
- Collaborative mindset with the ability to work in global teams.
- Strategic thinking with the ability to make data-driven decisions.
- Commitment to quality, integrity, and continuous improvement.
How to Apply for the Clinical Data Manager Role?
Interested candidates can apply directly through the Novotech Careers Portal. Applicants are encouraged to submit a detailed CV highlighting their experience in clinical data management and familiarity with regulatory data processes.
