Clinical Trials Coordinator
2 weeks ago
About the Job
As a Clinical Trials Specialist at Lifelancer, you will be responsible for leading the initiation and management of clinical trials at various healthcare facilities. Your key responsibilities will include preparing documentation for seeking permission to initiate clinical trials, managing the healthcare facilities' requirements, needs, and help needed, and delivering results that have a direct impact on the successful completion of the clinical program.
Key Responsibilities:
- Prepare documentation for seeking permission to initiate clinical trials.
- Manage the healthcare facilities' requirements, needs, and help needed.
- Deliver results that have a direct impact on the successful completion of the clinical program.
- Coordinate with PM and communicate progress and critical issues that may impair trial progress.
- Train and guide site staff in the protocol and trial procedures to minimize protocol deviations (PDs).
- Train site staff in safety information handling devices and systems.
- Monitor, review, and maintain the database in an organized system.
- Identify potential risks/difficulties and proactively take action to prevent or mitigate them.
- Ensure collaboration with and deliverables from.
- Collection and management of essential documents.
- Team involvement and participation in meetings.
Preferred Qualifications:
- Biomedical Engineer/Nursing /BAMS/BHMS or any relevant bachelors degree.
Core Competencies:
- Project Management skill set.
- Problem-solving.
- Decision making.
- Delegation skills.
- Relationship Management and influencing skills.
- Oral and written communication.
- Time management.
- Business English.
- Organizational and planning skills.
- Ability to work effectively in a team/matrix environment on multiple projects.
- Proven ability to work independently and effectively handle multiple priorities in a fast-paced environment.
- Demonstrable Risk Management skills.
- Delivery and risk-focused.
- Adaptability and Flexibility.
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