Are you looking for your next opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression? If so, come and join us!We are looking for experienced candidates to perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). This role will be supporting on-site the clinical research study for 24h/week.
Providing clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data
Attend all relevant study meetings
Collect and submit regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical research
Recruit and screen patients for clinical trials and maintain subject screening logs
Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits
Design and maintain source documentation based on protocol requirements
Schedule and execute study visits and perform study procedures
Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness
Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics
Monitor subject safety and report adverse reactions to appropriate medical personnel
Correspond with research subjects and troubleshoot study-related questions or issues
Assist with study data quality checking and query resolution
Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring
Record, report and interpret study findings appropriately to develop a study-specific database
Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards
Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records
Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies
Assist research site with coverage planning related to staffing and scheduling for research projects.
We are looking for candidates with the following skills and experience:
BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
Knowledge of medical terminology
Knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Must have previous experience of EDC entry and query resolution
Ability to pay close attention to detail
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
Good organizational skills with the ability to pay close attention to detail.
#LI-CES and #LI-DNP #ONSITEIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoeIQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-statusThe potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.EEO Minorities/Females/Protected Veterans/Disabled