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. Â
- Vacancy details:
- Department : Clinical Data Associate Trainee
- Qualification: Graduate in life science or pharmacy or clinical researchÂ
- Experienced: Relevant experience
Job Description: Greeting from Novotech !!!!
Important Details :
- Location : India
- Post of date 19/09/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face
- Interview Rounds of Interview: HR
Job Description
Brief Position Description:
The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Associate Trainee (CDA-Trainee) will be responsible for performing data entry, review, coding, and administrative support to CDMs on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).
Minimum Qualifications & Experience:
Graduate in life science or pharmacy or clinical research related field or similar. Relevant experience/qualification in allied professionals may also be considered. Preferably with good understanding of clinical research and data management process.Â
Responsibilities:Â
- The Clinical Data Associate Trainee will be responsible for providing accurate data acquisition, data validation, coding and reconciliation to the clinical studies and shall ensure quality in accordance with Novotech standards.
- Data entry of clinical trial data using Clinical Data Management software.
- Assist CDM with data cleaning/validation and reconciliation of external data.
- Tracking of CRF pages received and entered, tracking of data queries sent received and entered.
- May coordinate activities related to coding and electronic data transfers and address resulting discrepancies.
- Assist CDM with database testing and edit checks testing as appropriate.
- Assist CDM to create reports, listings, and other output as required during the project.
- Participation in project meetings as requested by CDM.
- Provide general admin support to Data Management according to the needs of the CDMs.
- Assist CDM in clinical coding and related data queries as appropriate.Â
- 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.

