Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
```Job Summary```
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our team. The Clinical Research Coordinator will be responsible for assisting in the coordination and management of clinical research studies. This role requires strong attention to detail, excellent communication skills, and the ability to work effectively in a fast-paced environment.
***It is essential to be bilingual, most of our patients are Spanish speaking, speak Spanish and English very well.***
-WE ARE LOOKING FOR A CRC BUT IF YOU HAVE EXPERIENCE IN RESEARCH DO NOT LIMIT YOURSELF, APPLY WE WOULD LIKE TO KNOW ABOUT YOUR SKILLS IN THIS CLINIC MODEL
You can write directly to info@novaresearchcenter.com (preferential)
```Responsibilities```
- Assist in the coordination and management of clinical research studies
- Ensure compliance with study protocols, regulations, and ethical guidelines
- Collect and document study data accurately and timely
- Conduct documentation review to ensure completeness and accuracy
- Manage data entry and data management processes
- Coordinate study visits, including scheduling appointments and preparing study materials
- Perform blood sampling and other specimen collection procedures as required
- Assist with the analysis of study data using statistical software
- Communicate with study participants, healthcare providers, and other stakeholders
- Maintain study records and files in accordance with regulatory requirements
```Skills```
- Strong attention to detail and ability to maintain accurate records
- Proficiency in data management and documentation review
- Knowledge of clinical trials management standards and regulations
- Experience with blood sampling techniques and specimen collection procedures
- Ability to analyze study data using statistical software
- Excellent organizational and time management skills
- Effective communication skills, both written and verbal
- Strong problem-solving abilities
If you are a motivated individual with a passion for clinical research, we encourage you to apply. We offer competitive compensation, professional development opportunities, and a supportive work environment. Join our team and contribute to groundbreaking medical research!
Please note that only qualified candidates will be contacted for further consideration.
Job Type: Full-time
Experience level:
Schedule:
Ability to Relocate:
Work Location: In person
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