CliniLaunch – Clinical Research Coordinator (CRC) Vacancy
Position Title:
Clinical Research Coordinator (CRC)
Company:
CliniLaunch
Qualifications:
B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
Experience Required:
0 Years / Freshers
Salary:
Not disclosed
Location:
Hyderabad, Bangalore, Chennai
Position Summary:
The Clinical Research Coordinator (CRC) is responsible for coordinating and administering clinical research activities under the guidance of the Principal Investigator (PI). The CRC ensures compliance with protocols, documentation accuracy, and adherence to regulatory requirements in clinical trials. This role involves managing daily operations, from patient recruitment to data reporting.
Key Responsibilities:
| Responsibility | Description |
|---|---|
| Participant Coordination | Recruit, screen, enroll, and follow up with participants. |
| Informed Consent | Obtain and ensure ethical standards in participant consent. |
| Documentation Management | Maintain case report forms, consent documents, and regulatory binders. |
| Protocol Implementation | Assist in developing and executing study protocols and procedures. |
| Adverse Events Monitoring | Report any adverse events and protocol deviations to PI and regulatory bodies. |
| Data Management | Ensure accurate data entry, quality control, and query resolution. |
| Participant Communication | Serve as the main contact for participant inquiries and concerns. |
| Study Coordination | Schedule visits, prepare materials, and collect biological samples. |
| Team Collaboration | Provide study updates and address issues in team meetings. |
| Study Closeout | Assist in data analysis, final reporting, and archiving of study materials. |
Qualifications:
- Bachelor’s degree in life sciences, nursing, public health, or a related field required; Master’s preferred.
- Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is highly desirable.
- Strong understanding of clinical trial processes, GCP, and regulatory requirements.
- Excellent organizational, time-management, communication, and interpersonal skills.
- Proficiency in Microsoft Office Suite and clinical trial management software.
