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```Overview:
We are seeking a highly organized and detail-oriented Study Coordinator to join our team. As a Study Coordinator, you will be responsible for ensuring that all research activities are conducted in compliance with FDA regulations and guidelines. This is an exciting opportunity for someone with a background in clinical research and data management to contribute to the advancement of medical knowledge.
Responsibilities:
- Ability to coordinate all aspects of clinical trials, including study design, protocol procedures, participant recruitment, and data collection
- Ensure compliance with FDA regulations, Good Clinical Practice (GCP) guidelines, and institutional policies
- Develop and maintain study timelines.
- Attend regular study team meetings to review progress, address challenges, and provide updates on study status
- Ability to collect and process biological samples, such as blood samples, in accordance with study protocols
- Ensure compliance with HIPAA regulations regarding the protection of patient privacy and confidentiality
-Ensure that patients rooms are clean and stocked appropriately.
-Some cleaning duties are a requirement.
Experience:
-Medical Assistant preferred but not a requirement
- Previous experience working in clinical research or a related field
-Knowledge of FDA regulations and GCP guidelines
- Experience in data management and analysis
- Familiarity with electronic data capture systems (EDC)
- Excellent organizational skills with the ability to manage multiple tasks simultaneously
- Strong attention to detail and accuracy
- Effective communication skills, both written and verbal
- Ability to work independently as well as collaboratively in a team environment
If you are passionate about advancing medical knowledge through clinical research and have the necessary skills and experience, we encourage you to apply for this exciting opportunity. Please submit your resume and cover letter detailing your qualifications and interest in the position.```
Job Type: Part-time
Pay: $12.00 - $12.50 per hour
Expected hours: 25 per week
Experience level:
Medical specialties:
Schedule:
Work Location: In person
Part Time
$41k-52k (estimate)
04/24/2024
05/15/2024
The job skills required for Study Coordinator part time include Clinical Research, Clinical Trial, Data Collection, HIPAA, Confidentiality, Data Management, etc. Having related job skills and expertise will give you an advantage when applying to be a Study Coordinator part time. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Study Coordinator part time. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Study Coordinator part time positions, which can be used as a reference in future career path planning. As a Study Coordinator part time, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Study Coordinator part time. You can explore the career advancement for a Study Coordinator part time below and select your interested title to get hiring information.