Clinical Research Coordinator - Franklin, United States - IQVIA
Description
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 usWe 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).
Day to day responsibilities will include:
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 dataAttend all relevant study meetingsCollect and submit regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical researchRecruit and screen patients for clinical trials and maintain subject screening logsOrient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visitsDesign and maintain source documentation based on protocol requirementsSchedule and execute study visits and perform study proceduresCollect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completenessHandle lab testing and analysis, including preparation of specimen collection tubes and lab logisticsMonitor subject safety and report adverse reactions to appropriate medical personnelCorrespond with research subjects and troubleshoot study-related questions or issuesAssist with study data quality checking and query resolutionPerform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoringRecord, report and interpret study findings appropriately to develop a study-specific databaseAssist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standardsAssist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training recordsPrepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agenciesAssist 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 settingKnowledge of medical terminologyKnowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedulesStrong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and WordMust have previous experience of EDC entry and query resolutionAbility to pay close attention to detailExcellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clientsGood organizational skills with the ability to pay close attention to detail.#LI-CES and #LI-DNPIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
Learn more at are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.'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.
potential base pay range for this role is $38.00-$50.00 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.