Job Description

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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