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Manager, Clinical Operations Jobs
Company | Jobot |
Address | La Jolla, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-08-10 |
Posted at | 10 months ago |
Want to learn more about this role and Jobot? Click our Jobot logo and follow our LinkedIn page!
Why join us?
Why join us?
- Monitor and track trial progress, identifying any potential issues or risks and implementing corrective actions to ensure trial milestones are achieved.
- Oversee the development and maintenance of the trial master file, ensuring accuracy and completeness of all essential documents.
- Collaborate with cross-functional teams, including clinical research associates, project managers, and data management teams, to ensure seamless coordination and execution of clinical trials.
- Conduct regular audits and inspections to ensure compliance with SOPs, regulatory guidelines, and industry best practices.
- Provide leadership and guidance to the clinical operations team, ensuring effective communication and collaboration to achieve project objectives.
- Stay up-to-date with the latest advancements and trends in clinical research, identifying opportunities for process improvement and implementing innovative strategies to enhance clinical operations.
- Ensure compliance with regulatory requirements and ethical standards, maintaining a high level of quality and integrity in all clinical operations activities.
- Develop and implement strategies to optimize clinical development processes, ensuring adherence to ICH GCP guidelines and standard operating procedures (SOPs).
- Oversee and manage all aspects of clinical operations, ensuring the successful execution of clinical research trials and projects within the scientific industry.
- Manage trial budgets and resources, ensuring efficient allocation and utilization to meet project timelines and deliverables.
- Minimum of 6 years of experience in clinical operations within the scientific industry.
- Detail-oriented with a high level of accuracy and attention to detail in all aspects of clinical operations.
- Proficiency in utilizing trial management systems and electronic data capture systems.
- Excellent organizational and time management skills, with the ability to prioritize and manage competing priorities effectively.
- Proven experience in managing multiple clinical trials simultaneously, with a track record of successful project delivery.
- Strong leadership and team management skills, with the ability to motivate and inspire teams to achieve project objectives.
- Exceptional communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and stakeholders.
- Strong knowledge and understanding of clinical research trials, clinical development, and ICH GCP guidelines.
- Bachelor's degree in a scientific discipline or related field. Advanced degree preferred.
- Ability to work independently and proactively, demonstrating a strong sense of initiative and problem-solving skills.
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