Q-Max is a reputed organization committed to excellence in clinical research and healthcare innovation. We specialize in conducting ethical and effective clinical trials that contribute to medical advancements. At Q-Max, you will be part of a dedicated team working towards impactful healthcare solutions.
Responsibilities of the Job
As a Clinical Research Coordinator, you will be entrusted with the following duties:
- Supporting and coordinating day-to-day clinical trial activities.
- Educating and guiding research volunteers about the trial process and participation rules.
- Monitoring medication administration or device usage during trials.
- Collecting and recording data, ensuring accuracy and adherence to trial protocols.
- Overseeing compliance with GCP, FDA requirements, and other regulatory guidelines.
- Participating in internal and external audits related to clinical trials.
Qualifications for the Role
To qualify for this position, candidates should have:
- A B.Sc/M.Sc in Clinical Research, B.Pharm/M.Pharm, or a related medical field (preferred).
- Familiarity with clinical trial protocols and medical terminology.
- Basic understanding of GCP and FDA policies (preferred but not mandatory).
- Freshers with a proactive attitude and eagerness to learn are welcome to apply.
Skills Required
The ideal candidate should demonstrate:
- Attention to detail to ensure accurate data collection and compliance.
- Strong communication and interpersonal skills to liaise effectively with trial participants and physicians.
- Proficiency in Microsoft Office and data capture systems (preferred).
- A collaborative and responsible approach to work.
How to Apply
Interested candidates can send their CVs to info@q-max.in
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