Clinical Data Associate Job Openings For Life Sciences at Novotech
Clinical Data Associate
India
Job Description
About the role:
Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements and Novotech/Client SOPs.
Minimum Qualifications & Experience:
Graduate in a clinical or life sciences related field. Relevant experience /qualifications in allied professions may also be considered. At least 2 years’ experience working in the research, pharmaceutical industry or a related field.
Responsibilities:
Member of the project team reporting to the Biometrics Project Manager on projects, the Clinical Data Associate is responsible for providing accurate data acquisition, data validation and reconciliation to the clinical studies and shall ensure quality standards per SOPs and ICH-GCP.
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Data entry of clinical trial data using Clinical Data Management software.
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Assistance in review of data queries to be raised with sponsor companies/monitoring staff.
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Tracking of CRF pages received and entered, tracking of data queries sent received and entered.
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Assist CDM with database testing and edit checks testing as appropriate.
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Assist CDM with data cleaning/validation and reconciliation of external data.
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Develop and maintain good communications and working relationships with lead CDMs.
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Assist CDM to create reports, listings, and other output as required during the course of the project.
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May coordinate activities related to coding and electronic data transfers, and address resulting discrepancies.
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Assist with the development and update of systems to track study progress as per the CDM requirements (i.e. Novotrak, CRF & query flow, safety reports, etc.). Provide updates on study progress to CDM as required.
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Participation in project meetings as requested by CDM.
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Assist with agenda/minute writing for data management teams.
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Adherence to company Quality Policy and procedures as applicable to carrying out job responsibilities.
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Provide general admin support to Data Management according to the needs of the Clinical Data Manager.
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Active contribution to company process improvement initiatives as assigned.
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Understand the responsibilities of Novotech as a service provider in the pharmaceutical industry and ensure all communications with external parties present a positive professional image of the company.
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Participation in industry fora (conferences, professional associations, etc) as a means of professional development as well as promotion of Novotech’s image in industry.
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Any other tasks associated with the day-to-day functioning of the DM Team as per the discretion and delegation of the Line Manager.
Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.
About Us
Novotech is a global full-service clinical Contract Research Organization (CRO).
Headquartered in Sydney, Australia, Novotech has 34 offices across Asia-Pacific, North America, and Europe. Novotech employs over 3000 employees and has over 5000 site partnerships and the resources and infrastructure to scale regionally and globally as clinical programs advance.
Novotech provides clinical development services across all clinical trial phases and therapeutic areas including feasibility assessments, ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management. Novotech obtained the ISO 27001 certification which is the best-known standard in the ISO family providing requirements for an Information Security Management System. Together with the ISO 9001 Quality Management system, Novotech aims at the highest IT security and quality standards for patients and biotechnology companies.
About the Team
At Novotech we have advanced therapeutic and regulatory expertise, the ability to execute across markets and a client-centric service model, so that our clients get a trusted, long-term partner and an accelerated path to bring their life-changing advances to market. This gives our employees the opportunity to develop their careers by joining a diverse and supportive global organization with a collaborative culture, whilst working with clients on the cutting-edge of life sciences.
At Novotech you will work alongside empowered teams with a shared commitment to success.
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Strategic vs transactional mindset.
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Ability to gain insights and make proactive decisions quickly.
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Culture that fosters partnership and collaboration, where every voice is heard and valued.
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Ongoing support from senior stakeholders and leadership team.
Job Info
Job Identification: 3430
Posting Date: 09/22/2025, 12:37 PM
Apply Before: 09/24/2025, 07:30 PM
Job Schedule: Full time
Locations: Ground Floor, Unit 1, Block E, Helios Business Park., Bangalore, 560103, IN
Keywords: Clinical Data Associate Job Openings For Life Sciences at Novotech. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebo
