Benefits: Competitive salary, 401(k), 401(k) matching, Dental insurance, Employee discount, Health insurance, Paid time off, Vision insurance
*Attention* all hard-working, responsible, and detail-oriented applicants:
Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction and supervision of the Principal Investigator.
Carry out clinical trial activities by adhering to Good Clinical Practice and study protocols
Maintain the integrity of data while protecting the rights, safety, and well-being of patients enrolled in clinical trials
Perform phlebotomy, EKGs, and obtain vital signs
Work closely with study monitors to coordinate and carry out Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits.
Complete Feasibility Questionnaires with PI and reach out to pharmaceutical and device companies to participate in new studies
Communicate with Institutional Review Boards to maintain the proper oversight of clinical trials
Assist with recruitment activities, consent patients, ensure eligibility prior to enrollment, and randomize subjects to study.
Ability to abstract data, complete timely case report forms and maintain research record and data integrity.
Maintains data in an audit-ready state
Ensures compliance to the research protocol, appropriate SOPs, policies and federal regulations while having a sound understanding of ICH/GCP guidelines and IATA requirements.
Must have excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately.
REQUIREMENTS: Two-year commitment required. In addition, this position requires:
Bachelor's Degree or three (3) years equivalent research experience
Minimum one year Research experience with two years preferred.
Certified Clinical Research Professional (CCRP) is preferred.
Experience with clinical trials is strongly preferred.
Knowledge of Institutional Review Board (IRB) policies and procedures.
Knowledge of the scientific method and statistical analysis techniques are preferred.
Microsoft Office computer skills required.
**Please submit cover letter to be considered for this position.
Investigate MD is a site associated with a private practice (Clear Dermatology and Aesthetics Center). We specialize in cosmetic, medical and procedural dermatology clinical research. We take pride in providing the highest possible quality of care, while providing a friendly and kind work environment.