Summary

The Margaret M. and Albert B. Alkek Department of Medicine at Baylor College of Medicine is seeking a highly motivated and detail-oriented [Title] to join our team. This role will manage and oversee a small group of clinical research and lipid clinic staff . Responsibilities include ensuring that the research is conducted ethically and in compliance with legal and scientific standards and BCM policies.  This role will also assist administrator with research budgets and monitoring department objectives. 

Job Duties

• Recruits, supervises, schedules, disciplines, and directs the daily activities of clinical research staff and private lipid clinic staff 
• Develops standard procedures for administering research and training staff.
• Provides feasibility and effort planning feedback to the principal investigator (Pl) and administration to help guide decisions regarding future clinic/research commitments
• Acts as liaison between Pl and research sponsors on regulatory quality control and quality assurance matters.
• Coordinates staff in the day to day activities of research protocols which includes screening, enrollment, and monitoring of research participants.
• Oversight for all CCDP Recruitment efforts: Conducts electronic medical records (EMR/EPIC) queries required for feasibility assessments for all CCDP trials under consideration and identifying potential candidates for studies.  
• Conducts weekly research and clinic staff meetings and provides minutes to all staff and medical director
• Responsible for IRB and institutional approvals.
• Coordinates all required start up activities for research protocols including ClinCard registration, TMH MORTI
• approvals as needed, local lab set up as needed, and BCM EPIC study set up.
• Organizes and plans team building events for all CCDP staff.
• Organizes clinic logistics and helps onboard staff and provide research training to the clinic lipid fellow as needed. 
• Performs other duties as assigned.
   

Minimum Qualifications

• High School diploma or GED.
• Four years of relevant experience.

Preferred Qualifications

• Bachelor’s degree. No experience required with Bachelor’s degree.
• Clinical research experience greater than five years.
• Computer proficiency in EPIC-electronic medical record system.
• Proficient knowledge in lab techniques; phlebotomy skills and lab safety.
• Experience with developing research source documents and standard operating procedures for administering research.
• Experience with regulatory procedures and preparation including IRB submissions for pharmaceutical clinical research.