Research Regulatory Coordinator
60K–80K a year
Behavioral Health Market Context
Apply Nowvia Learn4Good
Benefits
Dental CoverageHealth Insurance
Job Description
ves which drives our exceptional, patient-centered care.
Responsibilities
• Prepare and submit regulatory documents for a variety of study types, under limited supervision
• Manage appropriate databases, websites, and clinical trial management systems
• Participate in the creation, implementation, and documentation of study-specific training
Minimum Qualifications
• Education:
Bachelor's degree
• Experience:
2 years’ experience
Preferred Qualifications
• Previous experience in clinical research or working with regulatory affairs
• Strong knowledge of federal policies regulating clinical trials
What’s In It For You
e’s, caring for people in the communities we serve is our mission – and this includes our own SLHS team. We offer a robust benefits package to support our teams both professionally and personally. In addition to a competitive salary and retirement plans, we ensure our team feels supported in their benefits beyond the typical medical, dental, and vision offerings. We care about you and have fantastic financial and physical wellness options, such as: on-site massages, on-site counseling via our Employee Assistance Program, access to the Personify Health Wellness tool, as well as other formal training and career development offerings to ensure you are meeting your career goals.
Equal
Employment Opportunity
St. Luke’s is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other status or condition protected by law.
• Please note:
this posting is not reflective of all job duties and responsibilities and is intended to provide an overview to job seekers.
#J-18808-Ljbffr
Responsibilities
• Prepare and submit regulatory documents for a variety of study types, under limited supervision
• Manage appropriate databases, websites, and clinical trial management systems
• Participate in the creation, implementation, and documentation of study-specific training
Minimum Qualifications
• Education:
Bachelor's degree
• Experience:
2 years’ experience
Preferred Qualifications
• Previous experience in clinical research or working with regulatory affairs
• Strong knowledge of federal policies regulating clinical trials
What’s In It For You
e’s, caring for people in the communities we serve is our mission – and this includes our own SLHS team. We offer a robust benefits package to support our teams both professionally and personally. In addition to a competitive salary and retirement plans, we ensure our team feels supported in their benefits beyond the typical medical, dental, and vision offerings. We care about you and have fantastic financial and physical wellness options, such as: on-site massages, on-site counseling via our Employee Assistance Program, access to the Personify Health Wellness tool, as well as other formal training and career development offerings to ensure you are meeting your career goals.
Equal
Employment Opportunity
St. Luke’s is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other status or condition protected by law.
• Please note:
this posting is not reflective of all job duties and responsibilities and is intended to provide an overview to job seekers.
#J-18808-Ljbffr
Qualifications
- •Bachelor's degree
- •2 years’ experience
Benefits
- •We offer a robust benefits package to support our teams both professionally and personally
- •In addition to a competitive salary and retirement plans, we ensure our team feels supported in their benefits beyond the typical medical, dental, and vision offerings
- •We care about you and have fantastic financial and physical wellness options, such as: on-site massages, on-site counseling via our Employee Assistance Program, access to the Personify Health Wellness tool, as well as other formal training and career development offerings to ensure you are meeting your career goals
Responsibilities
- •Prepare and submit regulatory documents for a variety of study types, under limited supervision
- •Manage appropriate databases, websites, and clinical trial management systems
- •Participate in the creation, implementation, and documentation of study-specific training
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