Clinical Data Associate-I
Company: ProRelix Research
Location: Pune, India
Experience: 0–1 Year
Number of Openings: 02
Position Summary
ProRelix Research is seeking a Clinical Data Associate-I to support clinical data management activities across clinical research projects. This role is ideal for recent graduates and early-career professionals looking to build a career in Clinical Research and Clinical Data Management. The successful candidate will contribute to data entry, validation, quality review, and data management processes while ensuring compliance with regulatory and company standards.
Key Responsibilities
Clinical Data Management
Perform clinical data entry, review, and validation activities.
Ensure accuracy, completeness, and consistency of clinical trial data.
Assist in data cleaning and discrepancy management processes.
Generate, track, and resolve data queries in collaboration with study teams.
Support database quality control and data review activities.
Compliance and Documentation
Maintain compliance with study protocols, SOPs, GCP guidelines, and applicable regulatory requirements.
Assist in the preparation and maintenance of study-related documentation.
Ensure timely and accurate completion of assigned data management tasks.
Cross-Functional Collaboration
Work closely with Clinical Operations, Biostatistics, Medical Writing, and other project stakeholders.
Participate in project meetings and support study deliverables within established timelines.
Qualifications
Education
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Biotechnology, Biochemistry, Microbiology, Clinical Research, or a related discipline.
Experience
0–1 year of experience in Clinical Research or Clinical Data Management.
Fresh graduates with relevant academic exposure are encouraged to apply.
Required Skills
Strong attention to detail and data accuracy.
Good analytical and problem-solving abilities.
Understanding of clinical research processes and clinical trial data.
Effective written and verbal communication skills.
Proficiency in Microsoft Office applications.
Ability to work collaboratively within a team environment.
Preferred Qualifications
Basic knowledge of Good Clinical Practice (GCP).
Familiarity with Clinical Data Management concepts and workflows.
Exposure to clinical research through internships, projects, or academic coursework.
Application Process
Interested candidates may submit their updated resume to:
Email: career@prorelixresearch.com
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