Amy De Sa Email and Phone Number

Responsibilities of staff in this job classification vary across operational groups and consist of all or some of the followingduties:• Collaborate with the Study Director/Coordinator to prepare for and execute assigned studies. Assist in ensuring thatstudy objectives are met on time, within budget and according to applicable regulations and quality standards.• Collect, record and maintain volunteer screening, check-in and study data according to study-specific protocol and SOPsensuring quality control for content, accuracy and completeness. Record, report and interpret findings appropriately todevelop study-specific database.• Prepare for clinical trials by organizing and labeling specimen collection tubes and containers, setting up equipment anddocuments, and planning logistical activity for procedures as per study protocol.• Perform a variety of complex medical procedures such as cannulation and cardiac telemetry monitoring. Cross train inthe laboratory, radiology, and spirometry testing• Monitor volunteer safety and report adverse reactions to appropriate medical personnel. Attend to volunteer requests.• Maintain and restock medical supplies as needed. Maintain cleanliness and sanitation of the unit.• Recruit and screen volunteers for trials and maintain volunteer database.• Provide training on study-specific topics and new clinical skills. Assist in ensuring compliance with staff trainingrequirements by auditing and maintaining training records. Contribute to development of employees' training plans byadvising managers of continuing education requirements and opportunities.• Participate in a variety of team quality improvement efforts as necessary, and all meetings and training.• Assist with planning related to staffing and scheduling. Assist in ensuring that work shifts are staffed as required bysourcing internal staff, updating the scheduling system, and notifying staff of assignments

Perform a variety of complex clinical procedures to collect, record, report and interpret data on volunteers enrolled and/orseeking enrollment in clinical studies according to standard operating procedures (SOPs). Monitor volunteer response toevaluate effect of investigational drug. Assist with daily workload planning and staffing. Train staff on on study-related topicsand new clinical skills. Incumbents in this job classification may specialize in particular aspects of this job such as training,staffing or study coordination, and may not be required to carry out all responsibilities indicated below on a day-to-day basis.

Cash Control, Stock roation, Shop Maintances

Data entry on to appropriate system. Liasing with apporpriate staff regarding on-going projects. Answering telephone calls and emails. Clinical Trial ExperienceQuintiles Clinical Trial ExperienceStudy Phase: Phase 1