Q-Max Clinical Research Services is a Site Management Organization willing to partner with the Clinical Research Organization, Pharmaceutical, Biotechnology, and Medical Device companies for a successful outcome in their drug development endeavors. Our aim is to be recognized as a company which provides our customers with unparalleled service, responsiveness, and results with our finest resource to ensure that we satisfy to specific and unique needs.
We are hiring a Clinical Research Coordinator to oversee, train, and educate people who volunteer to participate in clinical trials for new medical drugs. In this role, it’s your responsibility to work with trial subjects and ensure that the research is done ethically. This includes making sure every aspect of the trial adheres to compliance, including GCP and FDA requirements and guidelines. In general, you must work closely with trial physicians to ensure the clinical trial process goes according to plan.
Job Openings for Fresher Candidates
- Location: Ahmedabad
- Interested candidates can send their CV on info@q-max.in
Clinical Research Coordinator Duties and Responsibilities:
- Support and coordinate day-to-day clinical trial activities
- Work with research volunteers about the trial and participation rules
- Oversee medication administration or device usage
- Conduct data collection and record reported results, as well as volunteer information
- Provide guidance on compliance with various guidelines and communicate any concerns
- Participate in audits
Clinical Research Coordinator Requirements and Qualifications:
- B.Sc/ M.Sc degree in clinical research, B.Pharm/ M.Pharm or a related medical field (preferred)
- Experience in a similar role, ideally coordinating patients
- Working knowledge of clinical trial protocols, medical terminology, and GCP and FDA policies
- Proficiency in Microsoft Office programs and data capture systems (preferred)
- Attention to detail
- Communication and interpersonal skills
