Step into a Rewarding Career as a Clinical Research Coordinator in Just Four Weeks
Master the skills required to coordinate clinical trials with confidence and precision. This focused four-week program equips you with essential knowledge in participant management, regulatory compliance, and site operations, setting you up for success as a Clinical Research Coordinator in the dynamic field of clinical research.
Key Features:
- 📋 Tailored Study Plans
- 📚 Real-World Case Studies
- ⏳ Program Length: 4 weeks
- 🖥️ Format: Bi-weekly, live-online sessions (1.5 hours each)
- ✔ Includes: Mock interviews, leadership coaching, weekly assessments
- 🎓 Certification Prep (Optional)
Structure
Week 1: Introduction to Clinical Research and GCP Essentials
Class 1: Fundamentals of Clinical Research and ICH-GCP Principles
- Overview of clinical research and its role in advancing healthcare.
- Understanding ICH-GCP guidelines and their importance in ethical clinical trials.
- Key principles of Good Clinical Practice (GCP).
Class 2: Roles and Responsibilities of a Clinical Research Coordinator (CRC)
- Overview of the CRC’s role in the clinical trial process.
- Relationships with investigators, sponsors, and monitors.
- Key responsibilities: documentation, participant management, and compliance oversight.
Week 2: Regulatory Compliance and Documentation
Class 1: Essential Documents and Good Documentation Practices (GDP)
- Definition and role of essential documents in clinical research.
- Trial Master File (TMF) and investigator site file (ISF) management.
- Good Documentation Practices (GDP) and ALCOA-C principles.
Class 2: Ethics Committees and Informed Consent
- Role of Institutional Review Boards (IRBs) and Ethics Committees (ECs).
- Types of review: full, expedited, and exempt.
- Informed consent process: principles, common deficiencies, and tips for compliance.
Week 3: Participant Safety and Data Management
Class 1: Adverse Events (AE) and Safety Reporting
- Definitions: Adverse Events (AEs), Serious Adverse Events (SAEs), and Adverse Device Effects (ADEs).
- Reporting timelines and compliance with global regulatory standards.
- Tools and workflows for accurate AE reporting.
Class 2: Source Data and Quality Data Management
- Ensuring the accuracy and reliability of source data.
- Strategies for managing case report forms (CRFs) and electronic data capture (EDC) systems.
- The role of ALCOA-C in data integrity.
Week 4: Audits, Leadership Development, and Career Preparation
Class 1: Preparing for Audits and Inspections
- Principles of GCP inspections and audits: purpose, scope, and possible outcomes.
- Preparing investigator sites for sponsor or regulatory audits.
- Post-inspection actions: addressing findings and implementing corrective action plans.
Class 2: Leadership Skills and Mock Interviews
- Developing leadership and communication skills for CRC roles.
- Resume building and interview preparation tailored for CRC positions.
- Simulated interviews with expert feedback to build confidence and competence.
Tangible Benefits:
- ✔ Career Readiness in 4 Weeks
- ✔ Resume and Interview Prep
- ✔ On-the-Job Support
Career Benefits:
- 💼 Hybrid Work Opportunities
- 💰 Salary Potential: $93,000 - $140,000
Special Launch Offer: $1,950 (Save 50%)
"Clinical Career Compass completely changed the way I approached my career. With no prior experience in clinical research, I lacked the confidence to even apply for CRC roles. Their mentorship provided clarity, actionable advice, and a clear understanding of site coordination. Within a month, I had secured my first job as a Clinical Research Coordinator, and my career has taken off ever since."
"I had no prior experience in clinical research, but Clinical Career Compass equipped me with everything I needed to succeed. The mentorship sessions and real-world examples helped me understand the responsibilities of a CRC and confidently step into the role. Just two weeks after completing the program, I started my first job in clinical research, and it’s been life-changing!"
