Clinical Data Manager

Clario Holdings Inc.; Bengaluru; Sur place; INR 1 200 000 - 1 800 000; Plein temps

Avantages offerts par ce poste

Competitive pay

Provident fund

Medical insurance

Remote work flexibility

Employee programs

Résumé du poste

Clario Holdings Inc. in Bangalore, India, is seeking a Clinical Data Manager to review and evaluate imaging-derived clinical data across trials, ensuring accuracy, compliance, and quality throughout the data lifecycle.

You will manage study setup, edit checks, data reconciliation, and documentation, collaborating with project teams while adhering to regulatory guidelines and SOPs; remote/hybrid options may be available.

Qualifications

• Bachelor’s degree in Life Sciences or related field; 3+ years in CDM.
• Relational database knowledge and validation experience.
• Familiarity with SAS desirable; proficient in Word/Excel/Access.
• Understanding of clinical trial terminology; attention to data quality.

Responsabilités

• Perform data management deliverables for assigned studies.
• Attend client meetings and understand study requirements.
• Develop and review edit checks; resolve discrepancies.
• Maintain study documentation and data lifecycle records.
• Coordinate data receipt and processing from external sources.
• Ensure regulatory compliance and SOP adherence.

Connaissances

Interpersonal communication

Problem-solving

Attention to detail

Team collaboration

Independent work

Formation

Bachelor’s degree in Life Sciences

Outils

SAS

Word

Excel

Access

Description du poste

## Clinical Data ManagerApplylocations: Bangalore, India: India Remotetime type: Full timeposted on: Posted Todayjob requisition id: R16967At Clario, part of Thermo Fisher Scientific. Join us as a global leader in clinical trial endpoint technology and help transform evidence generation for better patient outcomes. As a Clinical Data Manager, you will review and evaluate clinical data generated from the imaging portion of sponsor clinical trials across diverse therapeutic areas, ensuring accuracy, compliance, and quality throughout the data lifecycle.**What We Offer*** Competitive pay and incentives* Provident fund and medical insurance* Engaging employee programs and local events* Modern office spaces and remote work flexibility**What You’ll Be Doing*** Perform all data management deliverables for assigned studies* Attend and participate in client meetings as requested* Understand requirements for study implementation and data collection* Collaborate with project teams to develop study-specific edit check criteria* Define, run, and review edit checks; resolve discrepant data* Maintain organized, complete, and up-to-date study documentation* Perform study setup including TF design, database structure, and specifications* Coordinate and document receipt and processing of electronic or ancillary data from external sources* Review data for errors and inconsistencies; collaborate to resolve issues* Track outstanding issues and follow up until resolution* Ensure CDM activities comply with regulatory guidelines* Adhere to SOPs and departmental standards; assist in SOP updates* Contribute to team efforts and explore opportunities to add value* Maintain technical and industry knowledge through training**What We Look For*** Bachelor’s degree in Life Sciences, or related field (or equivalent experience)* 3+ years of experience in clinical data management within pharma, biotech, or CRO industry* Working knowledge of relational database organization and validation* Familiarity with SAS desirable* Proficiency with Word, Excel, and Access preferred* Understanding of clinical trial terminology desirable* Strong problem-solving skills and attention to detail* Ability to work independently and in a team setting; adaptable to changing priorities* Excellent interpersonal and communication skills* Strong documentation and organizational abilities* Based in or able to work from India (remote/hybrid options available)At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.