Home Study Case Manager
By Rising Ground, Inc At , Yonkers, 10705 $61,400 a year
Bachelor of Social Work (BSW) degree or an equivalent degree in education, psychology, sociology, or other behavioral science.
Two years’ experience working with youth in the social service field.
Knowledge of child welfare and immigration related legislation
Excellent verbal, written communication and organizational skills are essential
Responsible for completing Home Studies assigned by the HS Supervisor meeting ORR expected timeframe.
Maintain ongoing consultation with the HS Supervisor of any obstacle or barrier to timely completion of the HS report.
Program Manager, Study Operations
By Verily At Dallas, TX, United States
Experience in study project management and prior management of contracted resources/CROs.
8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager.
Deep knowledge of the range of tools used in the clinical study management space and associated technology solutions.
Identify and mitigate risks and apply strong problem-solving skills to ensure timely resolution of all project-related issues.
BA/BS/BScN degree in health or biologic science, or equivalent practical experience.
Master's degree in health or biologic science, or equivalent practical experience.
Home Study Writer Jobs
By CK Family Services At , Uvalde, 78801, Tx $275 - $400 a week

Thank you for your interest in partnering with CK Family Services to complete professional assessments of families and children. Specifically, this position is a subcontractor for CK Family Services ...

Patient Registry Study Manager
By Reata Pharmaceuticals, Inc. At Plano, TX, United States
Assist in the management and tracking of study-specific site payments
Working knowledge and experience with Word, PowerPoint, and Excel
Manage and maintain clinical and non-clinical supplies
Additional duties and responsibilities as assigned
2+ years of accumulated clinical trial support experience, which may include Site, CRO, Pharma, Biotech, and/or IRB-related experience
GCP and regulatory knowledge including FDA and ICH regulations

Are you looking for an exciting opportunity to manage preclinical studies? We are looking for a Preclinical Study Manager to join our team and help us develop innovative treatments for patients. You will be responsible for the planning, execution, and reporting of preclinical studies, ensuring that all studies are conducted in accordance with applicable regulations and guidelines. If you have experience in preclinical study management and are looking for a challenging and rewarding role, this could be the perfect opportunity for you!

Overview:

A Preclinical Study Manager is responsible for the planning, coordination, and execution of preclinical studies. This includes overseeing the design, implementation, and analysis of preclinical studies, as well as the management of study budgets, timelines, and resources. The Preclinical Study Manager is also responsible for ensuring that all studies are conducted in accordance with applicable regulations and guidelines.

Detailed Job Description:

The Preclinical Study Manager is responsible for the planning, coordination, and execution of preclinical studies. This includes overseeing the design, implementation, and analysis of preclinical studies, as well as the management of study budgets, timelines, and resources. The Preclinical Study Manager is also responsible for ensuring that all studies are conducted in accordance with applicable regulations and guidelines. The Preclinical Study Manager is responsible for the development of study protocols, the selection and management of study sites, the coordination of study activities, and the management of data collection and analysis. The Preclinical Study Manager is also responsible for the preparation of study reports and presentations, as well as the communication of study results to internal and external stakeholders.

What is Preclinical Study Manager Job Skills Required?

• Excellent organizational and project management skills
• Strong knowledge of preclinical study design and implementation
• Ability to develop and manage study budgets
• Ability to develop and manage study timelines
• Ability to develop and manage study protocols
• Ability to select and manage study sites
• Ability to coordinate study activities
• Ability to manage data collection and analysis
• Ability to prepare study reports and presentations
• Ability to communicate study results to internal and external stakeholders
• Knowledge of applicable regulations and guidelines

What is Preclinical Study Manager Job Qualifications?

• Bachelor’s degree in a scientific field
• 5+ years of experience in preclinical study management
• Experience in the pharmaceutical or biotechnology industry
• Knowledge of Good Laboratory Practices (GLP)

What is Preclinical Study Manager Job Knowledge?

• Knowledge of preclinical study design and implementation
• Knowledge of study budgets, timelines, and protocols
• Knowledge of data collection and analysis
• Knowledge of applicable regulations and guidelines
• Knowledge of Good Laboratory Practices (GLP)

What is Preclinical Study Manager Job Experience?

• 5+ years of experience in preclinical study management
• Experience in the pharmaceutical or biotechnology industry

What is Preclinical Study Manager Job Responsibilities?

• Plan, coordinate, and execute preclinical studies
• Oversee the design, implementation, and analysis of preclinical studies
• Manage study budgets, timelines