Clinical Trial Manager - Senior Clinical Trial Manager
Description:
• The Clinical Trial Manager (CTM) is a key member of Clinical Operations and will closely partner with the Associate Director, Clinical Program Management.
• Assist Clinical Program Manager with set-up of regional CRO and other vendors as required, including liaising with Global CRO to ensure site training and timely initiation.
• Day-to-day contact with counterpart at CRO and/or trial site; daily review and identification of potential issues or problems with the sites and communicates/escalates to Clinical Program Manager.
• Proactively identifies potential operational challenges and in collaboration with senior team members provides solutions to ensure study execution remains on track.
• Under supervision may serve as the key operational contact for Akero studies aiding in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
Requirements:
• At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
• At least 4+ years of experience and an RN (2 or 3 year certificate)
Benefits:
• Below is the pay range for this position that we reasonably expect to pay. Individual compensation is based on a number of factors including, experience, education and skill set, and geographic location.
• This range is for the San Francisco Bay Area, California location and may be adjusted to the labor market in other geographic areas.
Apply Now
Apply Now
• The Clinical Trial Manager (CTM) is a key member of Clinical Operations and will closely partner with the Associate Director, Clinical Program Management.
• Assist Clinical Program Manager with set-up of regional CRO and other vendors as required, including liaising with Global CRO to ensure site training and timely initiation.
• Day-to-day contact with counterpart at CRO and/or trial site; daily review and identification of potential issues or problems with the sites and communicates/escalates to Clinical Program Manager.
• Proactively identifies potential operational challenges and in collaboration with senior team members provides solutions to ensure study execution remains on track.
• Under supervision may serve as the key operational contact for Akero studies aiding in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
Requirements:
• At least 4+ years of relevant experience and a BS or BA in a relevant scientific discipline OR
• At least 4+ years of experience and an RN (2 or 3 year certificate)
Benefits:
• Below is the pay range for this position that we reasonably expect to pay. Individual compensation is based on a number of factors including, experience, education and skill set, and geographic location.
• This range is for the San Francisco Bay Area, California location and may be adjusted to the labor market in other geographic areas.
Apply Now
Apply Now