IQVIA

Senior/Clinical Research Associate (Client Dedicated)

Vietnam · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerIQVIA
  • LocationVietnam
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion opportunities and awards. Joining IQVIA will give you access to cutting-edge in-house technology and provide opportunities to work on global projects/ trials. You will be building a flexible, meaningful and fulfilling career with no limits.

Your responsibilities will include:

Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation

Supporting the development of a subject recruitment plan

Show full description

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. You will need to have a good knowledge of applicable clinical research regulatory requirements.

Qualifications:

University degree in scientific discipline or healthcare

At least 1 year of on-site monitoring experience

Good knowledge of GCP and clinical research regulatory requirements

Good computer skills including MS Office

Excellent command of English language

Organizational, time management and problem-solving skills

Ability to establish and maintain effective working relationships with colleagues, managers, and customers.

Flexibility to travel.

What you can expect:

Working with different customers on global trials

Career development opportunities for those who are passionate in wanting to grow as part of the organization.

Leaders that support flexible work schedules/arrangement

Excellent working environment in a stable, international, reputable company

Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape

Attractive remuneration package.

#LI-Hybrid

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 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.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

At a glance

  • Employment typeFull time
  • SenioritySenior
  • Employer posted
  • Added to ROLIVA
  • Last checked

Skills in this posting

Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.

GCP

Explore similar roles

Similar jobs