Job Title: Clinical Research Coordinator
Location: Mumbai
About Oxygen Clinical Trial
Oxygen Clinical Trial is a dynamic and growing organization dedicated to advancing healthcare through rigorous and ethical clinical research. We are currently seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team in Mumbai. This is an exceptional opportunity for recent graduates and experienced professionals in life sciences, pharmacy, or biotechnology to contribute to meaningful research and build a rewarding career in the clinical research field. If you are passionate about clinical trials and thrive in a fast-paced environment, we encourage you to apply.
Job Summary:
We are seeking a Clinical Research Coordinator to manage and coordinate the day-to-day activities of an ongoing clinical trial project in Mumbai. The CRC will work closely with the Principal Investigator (PI) and research team to ensure the study is conducted in accordance with the study protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The ideal candidate will possess strong organizational, communication, and interpersonal skills, as well as a solid understanding of clinical research principles.
Key Responsibilities:
- Trial Management: Oversee and manage the day-to-day operations of the clinical trial, ensuring smooth and efficient execution.
- Participant Recruitment and Enrollment: Assist the Principal Investigator (PI) in identifying, recruiting, consenting, screening, and enrolling eligible participants into the clinical trial. This includes explaining the study to potential participants, answering their questions, and obtaining informed consent.
- Protocol Adherence: Ensure strict adherence to the study protocol, GCP guidelines, and all applicable regulatory requirements.
- Adverse Event Reporting: Accurately and promptly report all Adverse Events (AEs) and Serious Adverse Events (SAEs) in accordance with established procedures.
- Communication and Collaboration: Communicate effectively and professionally with the CRO (Contract Research Organization), PI, investigators, Ethics Committee, and other stakeholders.
- Site Visits and Audits: Participate in site visits, audits, and inspections conducted by regulatory authorities, sponsors, or the CRO.
- Data Management: Collect, record, and maintain accurate and complete study data, ensuring data integrity and confidentiality.
- Reporting and Updates: Prepare and share regular updates and reports with the clinical research team and management, highlighting progress, challenges, and potential solutions.
- Documentation: Maintain organized and up-to-date study files, including regulatory documents, participant records, and communication logs.
Qualifications and Experience:
- Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or Biotechnology.
- Experience: Fresh graduates and experienced candidates are encouraged to apply.
- Location: Candidates based in Mumbai (preferred) or Kolkata candidates willing to relocate.
- Skills: Strong communication (both written and verbal) and documentation skills are essential.
- Knowledge: Understanding of GCP (Good Clinical Practice), clinical trials, and ethical principles is a significant advantage.
- Attributes: Must be detail-oriented, organized, and able to work independently as well as part of a team.
- Computer Skills: Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) is required.
Benefits of Joining:
- Real-World Experience: Gain hands-on experience in real-time clinical trial operations.
- Exposure and Networking: Obtain exposure to CRO coordination, regulatory compliance, and Ethics Committee interactions.
- Expert Mentorship: Work alongside industry experts and acquire strong clinical research experience.
- Competitive Compensation: Receive a competitive salary based on experience and qualifications.
- Career Growth: Enjoy a full-time, stable role with opportunities for professional growth and advancement within the company.
- Impactful Contribution: Contribute to the advancement of medical knowledge and patient care.
How to Apply:
If you meet the qualifications and are interested in joining our team, please submit your updated CV to [email protected]. We look forward to reviewing your application and discussing this exciting opportunity with you.