Clinical Data Manager I
Location: Bengaluru, Karnataka, India
Work Mode: Hybrid
Job Type: Full-Time
Function: Clinical Operations | Data Management
About Excelya
Excelya is a fast-growing, mid-size Contract Research Organization (CRO) committed to transforming healthcare through audacity, care, and energy. With a strong global presence and a workforce of over 900 professionals, Excelya delivers integrated clinical research solutions across full-service, functional service provider (FSP), and consulting models.
At Excelya, innovation, collaboration, and individual growth go hand in hand. The organization fosters a diverse and inclusive culture where professionals are empowered to make a meaningful impact on clinical research and patient outcomes.
Job Overview
The Clinical Data Manager I will play a key role in supporting end-to-end clinical data management activities for clinical trials. This position is ideal for early-career data management professionals who are eager to grow within a dynamic CRO environment and contribute to high-quality, compliant clinical research programs.
Key Responsibilities
Support clinical data management activities across the full study lifecycle, including study start-up, conduct, and close-out
Maintain clinical trial databases and ensure accurate clinical data flow across systems
Perform data review, data cleaning, and query management to ensure data integrity and quality
Support the design, review, and maintenance of electronic Case Report Forms (eCRFs)
Ensure compliance with ICH-GCP, FDA, EMA, and other applicable regulatory guidelines
Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Medical Writing
Support database lock activities and contribute to timely study deliverables
Maintain study documentation in accordance with SOPs and regulatory requirements
Qualifications & Experience
Education: Bachelor’s degree in a Scientific or Life Sciences discipline (preferred)
Experience Required: Minimum 1 year of experience as a Clinical Data Manager or an equivalent combination of education, training, and relevant experience
Required Skills & Competencies
Working knowledge of ICH-GCP and applicable ICH, EU, and FDA regulatory guidelines
Hands-on experience with clinical trial databases, data review processes, and eCRF design
Understanding of clinical trial processes and the clinical study lifecycle
Strong attention to detail with a focus on data accuracy and quality
Excellent verbal and written communication skills in English
Ability to work collaboratively in cross-functional and multicultural teams
Strong organizational and time-management skills
Why Join Excelya
Opportunity to work with a rapidly growing, innovation-driven CRO
Exposure to diverse clinical research projects across therapeutic areas
Collaborative work environment that supports learning and career progression
Inclusive workplace culture focused on diversity, equity, and respect
Chance to contribute directly to improving patient outcomes through quality clinical research
Our Culture: Excelling with Care
At Excelya, care is central to everything we do. We are committed to providing equal opportunities and fostering a workplace where diverse perspectives are valued. We encourage bold thinking, support professional growth, and work together to turn ambitious ideas into meaningful outcomes.
Apply now on thepharmadaily.com and take the next step in your Clinical Data Management career with Excelya.
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