Clinical Trial Coordinator
Are you passionate about making a difference in the world of pharmaceutical research? Do you thrive in a fast-paced, dynamic environment? Look no further, PPD-Pharmaceutical Product Development is seeking a talented Clinical Trial Coordinator to join our team. As a global leader in the clinical research industry, PPD is dedicated to delivering life-changing therapies to patients worldwide. In this role, you will play a crucial role in supporting the execution of clinical trials and ensuring their success. If you possess strong organizational skills, attention to detail, and a commitment to quality, we encourage you to apply for this exciting opportunity. Join us in our mission to improve health and save lives through innovative research.
- Coordinate and support the execution of clinical trials in accordance with established protocols and procedures.
- Ensure timely initiation, enrollment, and completion of clinical trials by effectively managing study timelines and milestones.
- Work closely with cross-functional teams, including study managers, clinical research associates, and investigators, to ensure smooth and efficient study conduct.
- Assist with the development and review of study documents, including protocols, informed consent forms, and study manuals.
- Monitor study progress and data quality, identifying and addressing any issues or deviations from protocol.
- Maintain study files and records in compliance with regulatory requirements and company policies.
- Facilitate study-related meetings and provide support for site initiation, monitoring, and closeout visits.
- Communicate with study sites and vendors to ensure timely and accurate completion of study activities.
- Assist with the preparation and submission of regulatory documents, such as IRB/EC submissions and IND/CTA applications.
- Contribute to the development and implementation of process improvements to increase efficiency and quality in clinical trial execution.
- Stay current with relevant regulations, guidelines, and industry best practices related to clinical research.
- Maintain a high level of professionalism and confidentiality in all interactions and communications.
- Actively participate in training and professional development opportunities to enhance job knowledge and skills.
- Foster a positive and collaborative team environment by actively contributing to team meetings and initiatives.
- Embody the company's core values and contribute to the overall mission of improving health and saving lives through innovative research.
Bachelor's Degree In A Science-Related Field Such As Biology, Chemistry, Or Pharmacology.
Certification In Clinical Research, Such As Ccra Or Ccrc, Preferred.
Minimum Of 3 Years Of Experience In Clinical Trial Coordination Or Management.
Strong Understanding Of Fda Regulations And Ich/Gcp Guidelines.
Excellent Organizational, Communication, And Problem-Solving Skills.
Communication Skills
Project Management
Time Management
Clinical Research
Budget management
Quality Control
Data collection
Regulatory compliance
Attention to
Patient Recruitment
Study Coordination
Protocol Adherence
Communication
Conflict Resolution
Leadership
Time management
Interpersonal Skills
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Trial Coordinator is between $60,000 to $90,000 per year. However, this can vary depending on factors such as location, experience, and the specific industry or company the individual is working for. Clinical Trial Coordinators with more experience and advanced degrees may earn salaries on the higher end of the range.
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PPD, Inc. is a global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.
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