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Open nowPosted 3 days ago

Senior / Clinical Research Associate

IQVIA RDS EAST ASIA PTE. LTD.

Pay
SGD 5,000 – SGD 10,000 a month
Where
Central, Singapore
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Your applicationOpen nowSenior / Clinical Research AssociateIQVIA RDS EAST ASIA PTE. LTD. · Central, Singapore

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  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on IQVIA RDS EAST ASIA PTE. LTD.'s own form.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 3 days ago

The posting

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
  • 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 4 years 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.

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