Are you passionate about clinical research and looking to advance your career in a dynamic and growing organization? CYTENET SMO is hiring Clinical Research Coordinators (CRC) for Mumbai, Pune, and Jaipur locations. With 3 vacancies available (one for each city), this is your chance to join a leading organization in the clinical research domain.
About CYTENET SMO
CYTENET SMO is a renowned clinical research organization dedicated to delivering high-quality clinical trial management services. We specialize in providing end-to-end solutions for clinical trials, ensuring compliance with global standards such as Good Clinical Practice (GCP) and ICH guidelines. Our mission is to contribute to the advancement of medical science by facilitating innovative and ethical clinical research.
Job Description
As a Clinical Research Coordinator (CRC), you will play a pivotal role in managing and overseeing clinical trials. Your responsibilities will include:
- Coordination and Oversight: Manage day-to-day operations of clinical trials, ensuring smooth execution.
- Participant Recruitment: Assist the Principal Investigator (PI) in recruiting, screening, and enrolling study participants.
- Informed Consent: Help the PI in obtaining informed consent from participants.
- Participant Visits: Schedule and conduct participant visits and follow-ups as per the study protocol.
- Data Collection: Accurately collect and record data in compliance with the study protocol.
- Compliance: Ensure adherence to study protocols, GCP guidelines, and regulatory requirements.
- Documentation: Maintain study documentation and ensure data integrity.
- EC Dossier Preparation: Assist in preparing Ethics Committee (EC) dossiers for submission.
- Stakeholder Communication: Liaise with CROs, sponsors, investigators, EC, and other stakeholders.
- Monitoring: Track study progress and report any issues or deviations to the PI or sponsor.
- Audits and Inspections: Participate in site visits, audits, and inspections as required.
- Reporting: Provide regular updates and reports to the clinical research team and management.
Qualifications and Experience
- Educational Background: Master’s or Bachelor’s degree in life sciences, healthcare, or a related field.
- Experience: 0.5–1.5 years of experience in clinical research or a related field (preferred).
- Knowledge: Familiarity with GCP, ICH guidelines, and regulatory requirements.
- Skills:
- Strong organizational and time-management abilities.
- Excellent communication and interpersonal skills.
- Attention to detail and accuracy in record-keeping.
- Proficiency in Microsoft Office and clinical trial management software.
Working Conditions
- Job Type: Full-time position.
- Location: Based in Mumbai, Pune, or Jaipur, with occasional travel to clinical sites.
- Training: Participation in ongoing training and development programs to enhance your skills.
How to Apply
If you are ready to take the next step in your clinical research career, submit your resume and cover letter to info@cytenet.org. Please mention the city you are applying for (Mumbai, Pune, or Jaipur) in the subject line of your email.
