Data Manager

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Are you seeking a purposeful and rewarding Data Management career opportunity?

Our Data Management team is growing in India, and with big ambitions and a clear vision for the future, now is the time to join Clario as a Data Manager.

These positions are subject to Indian, European and US working hour shift patterns, and are considered hybrid remote working roles from our offices in VG Heritage, 18/2, 18/3, Vani Vilas Road, Basavanagudi, Bangalore 560004.

What we offer:

• Competitive compensation + shift allowances

• Attractive benefits (security, flexibility, support and well-being)

• Engaging employee programs

• Technology for hybrid working and great onsite facilities

What you'll be doing:

The Data Manager is responsible for ensuring high quality data is obtained, processed and reported to Sponsors and defines the methods and tools Clario uses to provide these services.  The Data Manager is the primary contact for all data-related issues for both internal and external teams.

Serve as the primary internal and Sponsor contact for Data Management questions, issues, or concerns including, but not limited to:

• Data collection

• Data cleaning

• Data delivery 

• Data reconciliation

• Database lock 

• Data Management activity timelines​​

Define the Data Management Plan (DMP):

• Collaborate with Sponsors to define study requirements.

• Determine standard edit checks necessary to ensure clean data and define new edit checks when standard checks are insufficient.

• Develop Query Guidelines and SEC rules to minimize the query burden on sites while ensuring accurate demography and visit information is obtained.

• Collaborate with internal teams on study setup requirements such as demographic collection and visit schedule requirements.

• Communicate contents and commitments in the DMP to the internal CDM teams.

• Complete data management related pages in EXPClario/iClinica.​​

Lead the development, review, and finalization of data transfer requirements:

• Provide or customize Clario standard file specifications, review and/or consult with Sponsor on Sponsor-defined specifications, and coordinate finalization and approval of file specifications between Sponsors and SAS Programmers.

• Maintain approved file specifications.

• Perform any required validation of file formats or data content.

• Submit SAS programming requests for data file creation or edit check creation.

• Generate sample data from live study data.

• Provide sample data and the Data Transfer Agreement to the Sponsor teams.

• Maintain the signed Data Transfer Agreement.

• Manage database lock activities and timelines with the Sponsor to ensure data integrity and deliverable timelines are met.​

Serve as primary point of contact for query escalation:

• Routinely review and resolve escalated queries.

• Provide consolidated escalated query listings to Sponsor teams.

• Resolve Sponsor or Site issues escalated through Customer Care.​

What we look for:

• BS/BA Degree in Life Sciences or related field preferred.

• Minimum of 4+ years Data Management or related experience preferably in a clinical research position.

• Proficient in Microsoft Office applications.

• Strong organizational, interpersonal, time-management, and problem-solving skills.

• Ability to manage multiple priorities.

• Strong attention to detail.

• Previous SAS or SQL exposure or experience a plus. 

• Ability to communicate effectively in English.