drjobs Senior CRA

Senior CRA

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Buenos Aires - Argentina

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

The Senior Clinical Research Associate (CRA) will play a crucial role in the planning execution and management of clinical trials. This position requires a highly skilled and experienced professional who can ensure the integrity of clinical data compliance with regulatory requirements and the overall success of clinical research projects.

While projects vary your typical responsibilities might include:

  • Performing site selection initiation monitoring and close-out visits plus maintaining appropriate documentation
  • Supporting the development of a subject recruitment plan
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Evaluating the quality and integrity of site practices escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions recruitment case report form (CRF) completion and data query resolution
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally you will also have a good basic knowledge of applicable clinical research regulatory requirements.

REQUIREMENTS

You should have:

  • A Bachelors degree in a health care or other scientific discipline or educational equivalent
  • At least 4 years of on-site monitoring experience.
  • Advanced in English.
  • In-depth knowledge of GCP ICH guidelines and regulatory requirements.
  • Strong organizational and time management skills.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
  • Willingness to travel as required.

If you want to make an impact in the global research market where we are working to make a real difference in patient health we ask you to apply now and join our team.

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


Required Experience:

Senior IC

Employment Type

Full-Time

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.