Are you passionate about clinical research and data management? Bioclinica, a leading name in clinical trial solutions, is hiring a Clinical Data Manager in Bangalore, India. This full-time role offers an exciting opportunity to work on cutting-edge clinical trials across various therapeutic areas, ensuring high-quality data for groundbreaking medical advancements. If you have a knack for detail, strong problem-solving skills, and a background in life sciences or computer science, this could be your next career move!
Key Responsibilities of a Clinical Data Manager
As a Clinical Data Manager at Bioclinica, you’ll play a pivotal role in ensuring the integrity and accuracy of clinical trial data, with a focus on imaging data. Your responsibilities will include:
- Database Management: Oversee clinical trial databases to meet project requirements, including study setup, designing database structures, and creating specifications.
- Data Quality Assurance: Review clinical data, identify errors or inconsistencies, and collaborate with project teams to resolve discrepancies.
- Edit Check Development: Define, run, and review study-specific edit checks to ensure data accuracy.
- Study Implementation: Understand study requirements, coordinate data collection, and maintain organized, up-to-date documentation.
- External Data Coordination: Manage receipt and processing of electronic or ancillary data from external sources like CROs, sponsors, or central laboratories.
- Regulatory Compliance: Ensure all data management activities adhere to regulatory guidelines and Bioclinica’s SOPs.
- Team Collaboration: Work with internal teams to resolve issues, contribute to departmental standards, and participate in SOP reviews.
- Continuous Learning: Stay updated with industry knowledge through company-sponsored training.
Qualifications and Skills
To excel in this role, candidates should meet the following requirements:
- Education: Bachelor’s degree in Computer Science, Life Sciences, or a related field (or equivalent experience).
- Experience: At least 1+ years in a similar role within the pharmaceutical, biotech, or CRO industry.
- Technical Skills: Working knowledge of relational databases and validation; familiarity with SAS is a plus.
- Software Proficiency: Experience with Microsoft Office tools (Word, Excel, Access) is preferred.
- Industry Knowledge: Understanding of clinical trial terminology is desirable.
- Soft Skills: Strong problem-solving abilities, excellent attention to detail, and effective communication skills (both verbal and written).
- Adaptability: Ability to work independently in a team setting and adjust to changing priorities.
- Professionalism: Maintain a positive attitude and strong organizational skills.
Benefits of Working at Bioclinica
Joining Bioclinica offers a range of benefits, including:
- Career Growth: Work on global clinical trials and gain exposure to cutting-edge therapeutic areas.
- Professional Development: Access company-sponsored training to stay ahead in the industry.
- Collaborative Environment: Be part of a dynamic team dedicated to advancing medical research.
- Work-Life Balance: Minimal travel (0-15%) and a supportive workplace culture.
