Are you a Registered Nurse interested in Clinical Trial work. IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy of a new medication. The. visits/hours can. be arranged to suit your current work schedule but...
Are you a Registered Nurse interested in Clinical Trial work. IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy of a new medication. The. visits/hours can. be arranged to suit your current work schedule but...
Job Overview. Perform diverse administrative duties for head of Line of Business (typically VP level) with broad business responsibilities on a global basis or major region, necessitating high level contact and exposure to highly confidential information requiring considerable use of tact, diplomacy, discretion, and judgment. Essential Functions. Schedule appointments as determined by priority. Prepare and compose correspondence and reports. Main...
IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies meaning a vast amount of career development opportunities are available. Our Site Activation Specialists work under moderate supervision, executing the feasibility, site identification, regulato...
The candidate will serve as a Quality Specialist for the Clinical Data Science (CDS) organization. The Quality Specialist is responsible for assessing and improving quality across the trial portfolio, working to implement best practices to ensure appropriate controls for Good Clinical Practice (GCP) during the implementation of new or updated systems and/or processes. The role will focus on the development of a Quality Control Management Plan and...
This Position is Remote in North America. The IQVIA CNS Center of Excellence, a hub of CNS clinical innovation, is growing. We are looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our CNS portfolio and advance this dynamic and rapidly expanding area of clinical development. The CNS Medical Strategy Lead is a subject matter expert with experience in clinical research and clinical tria...
Job Overview. Secure and retain business through professional, consultative, proactive sales activities directed at decision-makers and decision influencers at existing and new clinical sponsors. Role can be Northeast based but frequent travel to the west coast will be required. Essential Functions. Actively prospect and leverage potential new business opportunities within specified customer account(s). Cultivate strong, long-term relationships w...
This is an on-site position in Mesa, Arizona. Overview. This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. Essential Functions. Develop stron...
IQVIA is seeking a CRA 2 with a minimum of 1.5 years of on-site oncology monitoring experience. Essential Functions. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive, and track subject recruitment plan in li...
Job Overview. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP)...
RESPONSIBILITIES. The role holder may be required to cover all or some of the responsibilities mentioned below but will be expected to focus on certain responsibilities for periods of time. Responsible for the development of complex investigator grant estimates, contracting strategies and proposal text to support the proposal development process. Develop contract and budget templates and contracting systems, tools, processes, and training materia...
IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies meaning a vast amount of career development opportunities are available. As Senior Site Activation Coordinator, under general supervision you will perform tasks at a country level associated wit...
