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Clinical Research Assistant - Egg Harbor/Pleasantville NJ

Posting date: 09/21/2022
  1. Part Time
R1326777

募集要項

この欠員は期限切れです。 下の同様の職務を参照してください...

Are you looking for an 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 whilst giving you the option of working flexibly?  If so, come and join us - IQVIA are looking Clinical Research Assistant.

This role, with an immediate start for 6 months is to support the site in Egg Harbor Pleasantville, NJ in part-time 24 hours per week (schedule 9am - 1pm).

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

 

Day to day responsibilities will include:

  • Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector

  • Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)

  • Preparing and maintaining study files, and timely submission of information

  • Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents

  • Scheduling visits with research subjects, generating appropriate reports and documentation

  • Other administrative support functions such as reception, office organization and supply management.

  

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 setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession 

  • Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

  • Basic knowledge of medical terminology

  • Experience in the field of respiratory disease would be a plus

  • Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

  • Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client

  • ​Good organizational skills with the ability to pay close attention to detail.

List #1

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