Amazing opportunity for an experienced Lead Clinical Research Coordinator or a SR CRC with leadership experience to move into a Management position in the Fort Collins 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 persite SOP's.
Ideal Experience:
- Minimum 4 years of research experience
- Minimum 1 years leadership experience
- Endocrinology exp a plus