Clinical Research Associate, Sponsor Dedicated job opportunity at IQVIA Holdings, Inc..

Home Jobs In United States Of America Tag: Sponsor Dedicated Clinical Research Associate, Sponsor Dedicated position at IQVIA Holdings, Inc.


DatePosted 30+ Days Ago bot
IQVIA Holdings, Inc. Clinical Research Associate, Sponsor Dedicated
Experience: 5-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Sponsor Dedicated

Copy Link Report
degreeBachelor's (B.A.)
loacation Durham, North Carolina, United States of America, United States Of America
loacation Durham, North ..........United States Of America

To be eligible for this position, you must reside in the same country where the job is located. Seeking experienced candidates near major hub airports in the Southeast, Northeast, Central and West regions. 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. Position requires 65-70% nationwide travel. 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 line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. MINIMUM RECRUITMENT STANDARDS: 2.5 years of clinical research coordination experience at site level Nursing or University Degree  (US Bachelor Level or equivalent)  in one of the life sciences Knowledge of electronic data capture preferred Equivalent combination of education, training and experience 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 $64,000.00 - $189,000.00. 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.

Other Ai Matches

Pharmaberater m/w/d Immunologie, Osteoporose Applicants are expected to have a solid experience in handling Osteoporose related tasks
Freelance- Translators/Linguists, Hungarian into English Applicants are expected to have a solid experience in handling Hungarian into English related tasks
Specialty Sales Representative, Specialty Medicines, Finland Applicants are expected to have a solid experience in handling Specialty Medicines, Finland related tasks
Freelance- Translators/Linguists, English into Spanish (Latin America) Applicants are expected to have a solid experience in handling English into Spanish (Latin America) related tasks
Principal Statistical Programmer, R Programming Applicants are expected to have a solid experience in handling R Programming related tasks
Pharmacy Tech Support Call Center Rep (Work from Home anywhere in the US) Applicants are expected to have a solid experience in handling Job related tasks
Local Trial Manager - Sponsor Dedicated Applicants are expected to have a solid experience in handling Job related tasks
Customer Success Manager Applicants are expected to have a solid experience in handling Job related tasks
FSP - Site Activation Manager in Argentina Applicants are expected to have a solid experience in handling Job related tasks
Aux. Enfermería Call Center (Supernumerario) Applicants are expected to have a solid experience in handling Job related tasks
Freelance- Translators/Linguists, English into French (Canada) Applicants are expected to have a solid experience in handling English into French (Canada) related tasks
MedTech Per Diem Clinical Educator- Dallas, TX Applicants are expected to have a solid experience in handling TX related tasks
Freelance- Translators/Linguists, English into Luo Applicants are expected to have a solid experience in handling English into Luo related tasks
Freelance- Translators/Linguists, English into Dutch(Belgium) Applicants are expected to have a solid experience in handling English into Dutch(Belgium) related tasks
Consultant, EMEA Strategy Consulting Applicants are expected to have a solid experience in handling EMEA Strategy Consulting related tasks
Patent Analyst Applicants are expected to have a solid experience in handling Job related tasks
Apotheken-Außendienst m/w/d 02 Schmerzmittel, inkl. Muskel- u. Gelenkschmerzmittel / OTC Applicants are expected to have a solid experience in handling inkl. Muskel- u. Gelenkschmerzmittel / OTC related tasks
Clin Trials Mtrl Technician Applicants are expected to have a solid experience in handling Job related tasks
CRA Line Manager Applicants are expected to have a solid experience in handling Job related tasks
FSP Principal Biostatistician - Chemistry, Manufacture and Control (CMC) Applicants are expected to have a solid experience in handling Manufacture and Control (CMC) related tasks
Mobile Medical Assistant/Phlebotomist-Per Diem In-Home Services Applicants are expected to have a solid experience in handling Job related tasks
Coordinador PSP Applicants are expected to have a solid experience in handling Job related tasks
Healthcare Trainer - Dysphagia Applicants are expected to have a solid experience in handling Job related tasks