Associate Clinical Data Reviewer at BIOCLINICA INC DBA CLARIS

Bengaluru, karnataka, India -

Full Time

Start Date

Immediate

Expiry Date

18 Jun, 26

Salary

0.0

Posted On

20 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Review, Data Management, Query Issuance, UAT, SOP Compliance, Problem Solving, Organizational Skills, Attention To Detail, Task Management, Communication Skills

Industry

Biotechnology Research

Description

At Clario, we are industry leaders in Medical Imaging and Specialty Solutions, supporting global clinical trials with high‑quality, reliable data. Our teams play a critical role in ensuring data integrity across complex studies, helping bring life‑changing therapies to patients faster. We are currently hiring multiple Associate Clinical Data Reviewers to join our Medical Imaging & Specialty Solutions team in Bangalore, India. These roles offer an excellent opportunity to begin or grow your career in clinical data management while working alongside a best‑in‑class global data team. What We Offer Competitive compensation Provident Fund & Gratuity Flexible leave plans Flexible work schedules and shift allowances Engaging employee programs Hybrid work environment What You’ll Be Doing Ensure the accuracy of client data by conducting manual data review for Clinical Data Management customers. Issue queries based on manual data review requirements for each assigned study. Participate in project team meetings as required. Generate metrics and reports reflecting the current state of the study database. Perform Clinical Data Management user acceptance testing (UAT) as needed. Adhere to Clinical Data Management processes and standards by using implemented systems. Read, understand, and comply with organizational Standard Operating Procedures (SOPs). Collaborate with internal teams to investigate and resolve data‑related issues. Contribute to team success by supporting colleagues and helping others achieve results. Identify opportunities to add value to departmental and organizational processes. Attend and participate in applicable company‑sponsored training to maintain and build technical and industry knowledge. Perform other duties as assigned. What We Look For Bachelor’s degree preferred. Minimum 1 year of experience in the pharmaceutical industry or other relevant experience. Strong problem‑solving and organizational skills. High attention to detail. Demonstrated ability to manage multiple tasks simultaneously and complete work within allocated time frames. Excellent oral and written communication skills. Fluency in English (both verbal and written) is required. 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 starting your clinical data career or building long‑term expertise, 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.

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Responsibilities

The Associate Clinical Data Reviewer will ensure data accuracy for Clinical Data Management customers by conducting manual data reviews and issuing necessary queries for assigned studies. Responsibilities also include generating database metrics, performing User Acceptance Testing (UAT), and adhering strictly to established processes and SOPs.