CAREER OPPORTUNITIES

Pharmaceutical Research Organization is continually recruiting qualified personnel to join our dynamic and innovative research team! If you enjoy working in a fast-paced, detail-oriented, patient-interactive, documentation-imperative position we would love to hear from you! Candidates should possess exceptional organization skills, friendly and outgoing personalities, problem-solving abilities, and superior knowledge in their related professional field.

We offer a highly competitive salary and benefit package to qualified employees. Available positions vary depending on current staffing needs. If you are interested in being considered for any of the positions listed below please forward your resume, any applicable professional licenses and salary history/requirements to Nancy Thomas, Executive Director at nthomas@rx-research.com.

Study Coordinator

RN, LPN, CMA, or background in health-related field. Minimum of 1 year clinical experience preferred. Current License required. CPR certification required.

Must possess exceptional organizational abilities, flexibility, desire for continuous knowledge and training, people-interactive capabilities (including interaction and problem-solving with physicians, mid-level practitioners, patients and their families, sponsor companies and their representatives, peers, and administrative officers) and be a self-starter. “Pride in workmanship” is imperative.

The study coordinator is responsible for the overall management of a clinical research trial. They are the “protocol expert” at their site. They are responsible for study start-up preparation, management and dispensing of study medication, potential patient screening, qualified patient enrollment, data gathering, documentation, patient scheduling and follow-up, personal quality assurance, meeting with sponsor representative for monitoring documentation, daily interaction and problem-solving with managers. Reports to the Clinical Team Manager.

Clinical Research Assistant

Background in health-related field preferred. Responsible for general research duties as assigned and supervised by a Study Coordinator. Reports to the Study Coordinator.

Quality Control

B.S., R.N., or background in health-related field preferred. Quality Control experience preferred. Responsible for quality control of patient information and data gathered during the clinical trial. Will verify accurateness of collected data, protocol compliance, Case Report Form transcription verification, GCP/ICH compliance, Code of Federal Regulations compliance, and regulatory accurateness and compliance. Reports to the Executive Director.