Research Associate - Start Up
Behavioral Health Market Context
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Job Description
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Please note that this position is in-office three days per week.
Responsibilities:
• Review clinical trial submissions and collaborate with Departments on completion and accurate submissions.
• Coordinate timely processing and compliant filing of clinical trial office documents, including regulatory documents.
• Assist clinical trial office team in weekly reporting and study status meetings with Departments and ensure study team compliance and completeness of pre-award processes.
• Assist in coordinating submission and notifications of clinical trials office processes and 3rd party vendor partners.
• Communicate study progress, critical updates, barriers or issues, modifications/amendment statuses, and any other important information to department and other stakeholders
Please note that this position is in-office three days per week.
Responsibilities:
• Review clinical trial submissions and collaborate with Departments on completion and accurate submissions.
• Coordinate timely processing and compliant filing of clinical trial office documents, including regulatory documents.
• Assist clinical trial office team in weekly reporting and study status meetings with Departments and ensure study team compliance and completeness of pre-award processes.
• Assist in coordinating submission and notifications of clinical trials office processes and 3rd party vendor partners.
• Communicate study progress, critical updates, barriers or issues, modifications/amendment statuses, and any other important information to department and other stakeholders
Qualifications
Benefits
Responsibilities
- •The Research Associate - Start Up will oversee the submission, review, and approval process of clinical trial protocols to the clinical trial office
- •This role involves providing formative feedback and support to Departments to ensure accurate, complete, and timely submissions
- •This role will also provide support throughout the various trial activation stages within the clinical trials office
- •Please note that this position is in-office three days per week
- •Review clinical trial submissions and collaborate with Departments on completion and accurate submissions
- •Coordinate timely processing and compliant filing of clinical trial office documents, including regulatory documents
- •Assist clinical trial office team in weekly reporting and study status meetings with Departments and ensure study team compliance and completeness of pre-award processes
- •Assist in coordinating submission and notifications of clinical trials office processes and 3rd party vendor partners
- •Communicate study progress, critical updates, barriers or issues, modifications/amendment statuses, and any other important information to department and other stakeholders
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