Job Title: Clinical Research Coordinator (CRC)
Location: Delhi/NCR, India
About Auxein Medical:
Auxein Medical is a leading medical device manufacturer committed to innovation and excellence in healthcare. We are dedicated to advancing medical technology and improving patient outcomes through rigorous research and development. As we expand our clinical trial operations, we are seeking a highly motivated and experienced Clinical Research Coordinator to join our growing team.
Summary:
We are seeking a dynamic and detail-oriented Clinical Research Coordinator to support our clinical research activities in the Delhi/NCR region. As a CRC, you will be responsible for managing all aspects of clinical studies, from site visits and patient enrollment to data management and regulatory compliance. This is an excellent opportunity for individuals with a strong background in clinical research, excellent communication skills, and a passion for advancing medical science.
Responsibilities:
- Conduct site visits to support ongoing research operations, ensuring adherence to protocols and regulatory guidelines.
- Admit patients into clinical studies, ensuring informed consent and accurate data collection.
- Perform real-time data uploads, maintaining data integrity and accuracy.
- Prepare and submit study documents to research sites and ethics committees, ensuring timely and compliant submissions.
- Maintain essential study documents, including study logs, case report forms (CRF), and records of adverse events (AE) and serious adverse events (SAE).
- Coordinate the availability of implants and instruments during research procedures.
- Manage the retrieval of study materials upon completion of clinical trials.
- Effectively communicate with and persuade patients to participate in clinical research studies.
- Travel between cities as required to support multi-site trials and ensure consistency in research operations.
- Monitor patient safety and report any adverse events according to established protocols.
- Collaborate with investigators and other research staff to ensure smooth and efficient study conduct.
- Maintain up-to-date knowledge of relevant regulations and guidelines.
- Assist in the preparation of study reports and presentations.
Qualifications:
- Bachelor’s or Master’s degree in Clinical Research or Biological Sciences.
- A minimum of 2 years of hands-on experience in clinical research coordination.
- Excellent patient communication and persuasion skills.
- Thorough knowledge of study documents, adverse event reporting, and site operations.
- Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Proficiency in data management and electronic data capture (EDC) systems.
- Strong organizational and time management skills.
- Ability to work independently and as part of a team.
- Willingness to travel frequently for study site visits.
- Excellent attention to detail and accuracy.
- Strong problem-solving skills.
Benefits:
- Opportunity to work with a leading medical device manufacturer.
- Exposure to real-world clinical studies and regulatory processes.
- Professional growth pathways in clinical operations and Research & Development.
- Permanent, full-time employment with stable career prospects.
- Competitive salary and benefits package.
- Collaborative and supportive work environment.
How to Apply:
If you are a highly motivated and experienced clinical research professional seeking a challenging and rewarding opportunity, we encourage you to apply. Please submit your resume and a cover letter outlining your qualifications and experience to [email protected]