Lead, Clinical Data Processor

At Clario, part of Thermo Fisher Scientific. Join us a global leader in clinical
trial endpoint technology and help ensure the highest standards of data quality
throughout our clinical study workflows. As Lead, Clinical Data Processor, you
will lead a team responsible for source document processing, query management,
quality checks, and workflow completion across multiple active clinical trials
within our Specialty Solutions division. Your leadership will ensure accuracy,
compliance, and operational excellence while supporting critical project
timelines for global sponsors. 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 Understand
and apply study‑specific redaction guidance, QC requirements, and GxP
expectations for source document processing Provision customer user accounts
across assigned studies and ensure compliance with access requirements Manage
and perform workflow events related to study execution, ensuring accuracy and
timeliness Review image, video, and document quality; perform redaction and
source preparation; facilitate translation or DICOM link creation when required
Issue queries and conduct routine follow‑up with study sites; escalate trends or
risks to Project and Operations Managers Assist with generating and distributing
final study closeout deliverables Monitor and balance team workload; drive
improvements to ensure timely and accurate task completion Oversee large,
multi‑staff tasks, ensuring quality and communication with Project Managers or
customers Support Project Support staff in communicating delays, issues, or
risks to internal or external stakeholders Collaborate with supervisors to
maintain procedures that meet internal, client, and regulatory requirements Lead
or participate in project/team meetings and guide staff on deliverables,
processes, and timelines Support Quality Assurance teams during sponsor audits
and follow‑up actions Partner with other departments to develop tools,
procedures, and training to strengthen the Project Support team Facilitate
cross‑functional interactions to ensure successful project execution Manage
expectations with Clario Project Management and customers for assigned tasks
Maintain strong professionalism, accountability, and quality in all deliverables
Ensure English‑language fluency across written and verbal communications Follow
SOPs, project‑specific instructions, and study documentation Participate in SOP
updates, team QRGs, and Work Instruction development Collaborate with internal
staff to resolve issues and support team success Maintain industry and technical
knowledge through training and ongoing learning What We Look For
Associate/Bachelor’s degree in Computer Science, IT, Life Sciences, or related
field (or equivalent experience) 3 + years of experience in clinical trials,
healthcare, or a related field; 1+ year clinical trial experience preferred
Proficiency with MS Office tools (Word, Excel, Teams, OneNote) Ability to
identify PII/PHI deviations and apply Good Documentation Practice for redaction
Exceptional attention to detail and accuracy Ability to work independently and
collaboratively, with strong judgement under pressure Strong organisational,
prioritisation, and problem‑solving skills Excellent interpersonal, written, and
verbal communication abilities Ability to maintain professionalism and a
positive attitude at all times Based in or able to work from Bangalore (on‑site
or hybrid) 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.
Clario Privacy Policy Clario is a leading provider of endpoint data solutions to
the clinical trials industry, generating high-quality clinical evidence for life
sciences companies. We offer comprehensive evidence generation solutions that
combine medical imaging, eCOA, precision motion, cardiac solutions and
respiratory endpoints. For more than 50 years, Clario has delivered deep
scientific expertise and broad endpoint technologies to help transform lives
around the world. Our endpoint data solutions have supported over 30,000
clinical trials in more than 100 countries. Our global team of science,
technology, and operational experts have supported over 70% of all FDA drug
approvals since 2015.