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, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals.

Key Responsibilities:

Coordinates advanced clinical research projects as the primary CRC on at least 4 studies of medium to high complexity, as well as back-up CRC on other studies when neededAssures that the integrity and quality of clinical research trials is maintained Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achievedOversees the work of research assistants and trains junior staff as appropriateWorks effectively with multidisciplinary, ancillary, and inter-professional research teamsFunctions independently, and is able to identify situations where additional support is necessaryCompletes all protocol related training Performs patient/research participant scheduling Collects patient/research participant medical history Collects and maintains source documentationManages inventory and administers test articles/investigational product to participantsPerforms data entry and query resolution Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.). Adheres to an IRB approved protocol Obtains informed consent of research subjectsSupports the safety of research subjects, report adverse events. Coordinates protocol related research procedures, study visits, and follow-up Facilitates site qualification, study initiation, and monitoring visits, and study close-out activities Ensures proper collection, processing, and shipping of laboratory specimens May be asked to perform special project responsibilities and travel to other locations when needs ariseComplies with Avacare, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelinesPerforms other duties as assigned

Required Knowledge Skills and Abilities:

Must demonstrate the ability to fulfill responsibilities of CRC Level I Knowledge and ability to apply GCP/ICH and applicable regulatory guidelinesKnowledge and experience of site operations and the drug development processExcellent written and verbal communication skills – must be comfortable and effective in communicating with potential study participants from a diverse population Interpersonal skills - open to others’ ideas and willing to learn new things; respond well to questions and challengesProcess improvement – support ideas and theories on process improvement for efficiency and effectivenessComputer proficiency in use of Microsoft Word, Excel

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 https://jobs.iqvia.com

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, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $36,600.00 - $91,300.00. 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.