Are you ready to advance your clinical data management career with a world-leading CRO? Quanticate, a global data-focused Clinical Research Organization (CRO), is hiring a Clinical Data Manager I in Bengaluru, Karnataka, India.
This full-time, on-site position offers the opportunity to manage end-to-end clinical data processes, ensuring quality, compliance, and regulatory excellence across global clinical studies. If you have 6–8 years of experience in CRO clinical data management, this could be your next big step in advancing your clinical research career.
Key Responsibilities
As a Clinical Data Manager I at Quanticate, your core responsibilities include:
- Leading and coordinating all clinical data management (CDM) tasks from study initiation to completion.
- Ensuring all CDM activities adhere to contractual agreements, SOPs, and GCP/ICH guidelines.
- Overseeing CRF management, medical coding, and data review processes.
- Managing study timelines, progress tracking, and resource allocation.
- Acting as the primary CDM contact for internal and external stakeholders.
- Supervising and mentoring assigned staff; conducting performance reviews and training.
- Supporting SOP creation, process improvement, and strategy development within CDM.
Required Qualifications
To qualify for this role, candidates should meet the following criteria:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related field.
- 6–8 years of experience in CRO Clinical Data Management, with study leadership exposure.
- Proficiency in Oracle Clinical, Medidata Rave, or Inform.
- In-depth understanding of ICH-GCP guidelines and data management regulations.
- Strong project management, client communication, and leadership skills.
- Proven ability to manage cross-functional teams and ensure quality data deliverables.
How to Apply
