Job Title

Job Title Clinical Research Coordinator Work Set-Up Working On-site Schedule 24 hours per week. Responsibilities Phlebotomy is required, and pediatric experience is also needed. Community outreach will be part of the role. Perform complex clinical procedures on subjects, including ECG, sample collection with spirometry, and vital signs. Coordinate clinical research studies conducted by a supervising principal investigator. Update and maintain skills, training and knowledge of current best nursing practices and topics related to clinical research. Safeguard the wellbeing of the subjects and ensure and maintain high standards: maintain a safe environment in accordance with Health and Safety policies; act as a volunteer advocate; address volunteer and visitor concerns proactively and take remedial action as required; assist staff, both registered and unregistered, in clinical coordination practices and delivery of care to volunteers; report any deviation from normal practice to senior staff. Support Study Conduct By Review the study protocol, case report form (CRF), other study documents and electronic data capture systems. Participate in project meetings with the project team as needed. Perform clinical setup and preparation for the study, including labeling specimen collection tubes, setting up equipment and documents. Plan logistical activity for procedures as per protocol.> Generate volunteer instructions. Identify and obtain required supplies and equipment. Prepare and deliver studyspecific training materials, documents and records. Troubleshoot study issues. Participate in huddles to ensure daily tasks assigned to team members are executed to expected standards. Assist with data quality checking and query resolution to ensure that data collected on study volunteers adhere to study protocol and ensure quality control for content accuracy and completeness. Recruit and screen volunteers for inclusion in the study based on predetermined criteria. Orient volunteers to the study and the site includes purpose of the study, procedures, and practical issues such as timelines for visits. Responsible for correct administration and custody of study drug according to site standard operating procedures. Collect, record and report clinical data and findings appropriately in case report forms (CRFs); collaborate closely with study investigator, inform on relevant adverse events and serious adverse events per protocol. Cooperate with the study monitor and reserve sufficient time for questions during monitoring. Follow ICH GCP guidelines with regard to all study and patient activities. Qualifications High School Diploma and 1 years relevant work experience in clinical research OR bachelors degree with 2 years of relevant work experience. At least 1 year experience working in a clinical research setting preferred. Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies. Working knowledge of clinical trials. Working knowledge of the principles of Good Clinical Practices (GCP). Indepth knowledge of protocol and studyspecific operating procedures, consent forms and study schedules. Skill in carrying out required clinical procedures. Working knowledge of medical terminology. Ability to pay close attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians and clients. Please note, this position is not eligible for sponsorship. #LI-CES and #LI-DNP #LI-HCP #ONSITE IQVIA 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 IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request. If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at , so that IQVIA can support your participation in the recruitment process. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. La fourchette salariale de base potentielle pour ce poste est de annuellement. Le salaire de base rel offert peut varier selon plusieurs facteurs, notamment les qualifications lies lemploi telles que les connaissances, les comptences, la formation et lexprience; lemplacement; et/ou lhoraire (temps plein ou temps partiel). Selon le poste offert, des rgimes dincitation, des primes et/ou dautres formes de rmunration peuvent tre proposs, en plus dune gamme davantages sociaux lis la sant, au bientre et/ou dautres bnfices. The potential base pay range for this role is The actual base pay offered may vary based on a number of factors including jobrelated qualifications such as knowledge, skills, education and experience; location; and/or schedule (full or parttime). 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. #J-18808-Ljbffr