Clinical Trial Assistants - full time, part time or flexible working hours available - Connecticut
Job details
Estimated: $46,000 - $62,000 a year
Part time
Benefits
Flexible schedule
Job description

Clinical Research Assistants / Clinical Trial Assistants - full time, part time or flexible working hours available - Connecticut


Are you looking for your next 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 for experienced site-based Clinical Research Assistants to work on a variety of upcoming projects in pharma, biotech and medtech.


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

  • Processing lab specimens, labelling vials, accurately filling out requisitions for storage and/or shipment per study protocol and shipment regulations

  • 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

  • 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 organisational skills with the ability to pay close attention to detail.


#LI-XB1

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

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Company details

Headquarters

Durham, NC

Employee

10000+

Revenue

more than $10B (USD)

Industry

Pharmaceuticals

Company Description
At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 82,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.
Company ratings
  • Overall
    3.8
  • Company & Benefits
    3.5 / 5
  • Culture & Values
    3.6 / 5
  • Career Opportunities
    3.3 / 5
  • Work/Life Balance
    3.7 / 5
  • Senior Management
    3.4 / 5
Company reviews
"Good place to work"
Former EmployeeCOVID-19 STUDY WORKER
Supportive environment with option to further your career if you so wish. Manager was very proactive, supportive and encouraging. I would definitely recommend this company.

"You'll go as far as your silo goes"
Former EmployeeAssociate Manager
If you are hired on a contract, if is hard to move up internally. Advice to management: if you are going to have leadership development programs, have a way to promote those employees that you spent money on to train.

"Well rounded "
Former EmployeeManagement Associate
Overall good company. As usual depends on whether you have good leadership directly above you as to whether you easily move up. Insurance benefits are pretty typical.

"worst corporate culture"
Current EmployeeSoftware Engineering Manager
The only positive part were the flexible working hours and the ability to skip office physical presence. But I was probably an exception and rather a lucky one because the rest didn't have that privilege! Apart from that, there is no structure in the organization. People get favored overnight because of their personal relationships. Also, they tend to acquire a lot of companies and everything can easily change the way your job gets done. My reporting manager was changed 6 times up to now! Overall, a big mess and no way to improve your personal career and enhance your skills. As an IT professional, that has a big impact. During the recruiting process, they try to shine with modern and up to date IT practices, but what you really find is a pure disaster. Not only the technical environment but also the quality of the people is well below average.
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