Job Title: Clinical Research Trainer
Company: CLRI - CliniLaunch Research Institute
Location: 3rd floor, Ozone Manay Tech Park, Kudlu Gate, Garebhavipalya, Garvebhavi Palya, Bengaluru, Karnataka 560068
Job Type: Full-Time
Company Website- https://clinilaunchresearch.in/
We are seeking a highly skilled and experienced Clinical Research Trainer to join our dynamic team. The ideal candidate will possess a deep understanding of clinical research principles, data management best practices, and regulatory compliance requirements. You will be responsible for designing, developing, and delivering comprehensive training programs to our employees, covering a wide range of topics within these domains.
Key Responsibilities:
- Training Program Development:
- Develop and implement a robust training curriculum aligned with industry standards and regulatory requirements.
- Create engaging training materials, including presentations, handouts, and online learning modules.
- Design and deliver customized training programs to meet the specific needs of different teams and individuals.
- Training Delivery:
- Conduct effective training sessions using a variety of delivery methods, such as instructor-led training, webinars, and e-learning.
- Facilitate interactive learning experiences, including group discussions, case studies, and role-playing exercises.
- Assess participant knowledge and skills through pre- and post-training assessments.
- Stay up to date with the latest regulatory guidelines and industry best practices.
- Ensure that all training programs are compliant with relevant regulations, such as Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Knowledge Transfer:
- Share knowledge and expertise with team members to foster a culture of continuous learning and improvement.
- Mentor and coach new employees to help them develop their skills and knowledge.
Qualifications and Skills:
- Advanced degree in a relevant field, such as life sciences, pharmacy, or public health.
- Extensive experience in clinical research, clinical data management, and regulatory affairs.
- Proven track record of designing and delivering effective training programs.
- Strong understanding of regulatory requirements, including ICH-GCP and FDA regulations.
- Excellent communication and presentation skills.
- Ability to adapt to different learning styles and tailor training content accordingly.
- Strong organizational and time management skills.
- If you are passionate about training and development, and have a strong understanding of clinical research, data management, and regulatory affairs, we encourage you to apply.
