What are the responsibilities and job description for the Clinical Research Site Manager position at SQRL?
Amazing opportunity for an experienced Site Manager, Lead Clinical Research Coordinator, or a SR CRC with leadership experience to move into a Management position in the Longmont area!
Highlights :
Heavy approach in training, learning, and development!
They currently have 18 clinical research sites - half of them are embedded into physician offices and the other half are stand-alone sites 100% dedicated to research.
The company is growing quickly, so there is a lot of room for promotion and growth
Mainly focused in vaccine and infectious diseases, but now expanding into endocrinology, neurology, and rheumatology.
Job Description :
You will be managing day-to-day site activities for optimization of site performance.
Responsible for driving the site to achieve company goals, client satisfaction, and patient care
Manage all day-to-day operations of the clinic and train and develop staff.
Organize all aspects of the clinical trials assigned and ensure success
Participate in investigator meetings, site initiation meetings
Work with our internal patient recruitment department for participant screening and enrollment and ensure compliance with protocol and all applicable regulations.
Conduct Informed consent process and conduct study related visits.
Monitor subjects per protocol requirements.
Assess, monitor, and report adverse events per protocol.
Maintain required records of study activity including source documentation, case report forms, drug dispensation records, and data management system entry.
Complete case report forms and resolve queries.
Provide assistance to fellow study coordinators including obtain, process and ship study related specimens
Manage quality assurance assigned protocols per site SOP’s.
Ideal Experience :
Minimum 3 years of research experience
Minimum 1 years leadership experience
Vaccine and Infectious Disease experience is a plus!
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