Clinical Research Coordinator (CRC)
ちけんこーでぃねーたー
Industry & Occupation
Classification
Summary
A professional at pharmaceutical companies or CROs who manages clinical trial progress, supports subjects, and ensures data quality management.
Description
Clinical Research Coordinators (CRCs) belong to pharmaceutical companies or CROs, handling clinical trial (clinical study) schedule management, protocol compliance confirmation, assistance with informed consent, support for case report form (CRF) creation, quality management (QA), and more. They collaborate with principal investigators, clinical development monitors (CRAs), and medical staff to conduct trials safely and appropriately in accordance with GCP and related regulations. Subject follow-up, adverse event reporting, and data collection/management are also important tasks.
Future Outlook
Demand is on an expanding trend with the increase in new drug development and global clinical trials. Expectation of growing needs for highly specialized personnel.
Personality Traits
Able to Pay Attention to Details / Excellent Communication Skills / Good at Coordination / Strong Sense of Responsibility
Work Style
Contract Trial Institution / Full-time / Pharmaceutical Company Employment / Remote Hybrid / Shift
Career Path
Assistant CRC → CRC → Senior CRC → Clinical Development Monitor (CRA) → Project Manager (Clinical Development) → Consultant
Required Skills
CRF Creation and Management / Clinical Trial Related Document Management / GCP Knowledge / Informed Consent Procedures / Trial Protocol Understanding
Recommended Skills
Basics of Statistics / CRO Work Experience / English Literature Reading / Team Management
Aptitudes (Strengths Preferred)
| Item | Description |
|---|---|
| Attention to Detail & Accuracy | Meticulous attention is required for data accuracy and regulatory compliance. |
| Communication Skills | Because it requires close collaboration and coordination with patients, medical staff, and monitors. |
| Learning Agility & Knowledge Acquisition | Need to continuously learn specialized knowledge such as GCP and related regulations. |
| Planning & Organization | Need to accurately manage clinical trial schedules and resource adjustments. |
| Collaboration & Teamwork | Because it advances clinical trials through collaboration with multiple professions. |
Aptitudes (Weaknesses Acceptable)
| Item | Description |
|---|---|
| Creativity & Ideation | The work follows norms and procedures, resulting in low degree of freedom. |
| Physical Stamina & Endurance | Involves extensive long-hour paperwork and facility visits, with minimal physical labor. |
Related Qualifications
- Certified Clinical Research Coordinator
- Nursing License
Aliases
- CRC
- Clinical Research Coordinator
- Clinical Trial Coordinator
Related Jobs
- Clinical Development Monitor (CRA)
- Clinical Research Coordinator
- Clinical Trial Monitor