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Clinical Research Associate II - FSP

China - Any Region - Home Based Date posted 05/18/2022 Job ID 79408BR

Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction.

As a CRA at Parexel, you‘ll be joining a team with a wide variety of experiences and knowledge. We’re looking for people like you to take the initiative to do things better and smarter—people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients. Explore opportunities within our core Clinical Development, Biotech, or Functional Service Provider (FSP) teams below.

Success Profile

Check out the top traits we’re looking for and see if you have the right mix.

  • Innovative
  • Problem-Solver
  • Communicator
  • Tech-Savvy
  • Confident
  • Independent
  • "The last 4.5 years I had a steep learning curve and I am still learning via on-the-job challenges and solid management feedback. Next to my personal growth, I also enjoy our open atmosphere and the great collegiality."

    Stefanie – Sr Clinical Research Associate


  • Global Impact

    We are one truly global team working together to propel each client´s journey ahead faster.

  • Balance

    We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

  • Collaboration

    Work with industry leaders and subject matter experts.

  • Freedom

    The ability to innovate, ask “what if” and try new solutions without fear of failure.

  • Variety

    Opportunities to work on multiple accounts – never boring!

  • Compensation

    Competitive salaries and bonus structure based on individual metrics.


Clinical Research Associates II (FSP)

Parexel FSP is currently seeking Clinical Research Associates II in Beijing, China

Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you. Expect exciting professional challenges on inspiring studies, but with time for your outside life.

Some specifics about this role
  • Primarily responsible for initiating, organizing and managing the assigned trials, ensuring the
  • trials can be conducted as per timeline requirement
  • On-site monitoring and site management for global studies
  • Ensure clinical trials are conducted in compliance with local, national and regional protocols
  • and ICH-GCP
  • Drives performance at site by proactively identifying and ensuring timely resolution to study
  • related issues and escalates them as appropriate.
  • Contributes to selection of potential investigators
  • May be accountable for study start-up and regulatory tasks, including from collection to tracking of documents for Site Qualifications visits, submission of proper documents to EC/IRB and Regulatory Authorities for start-up and throughout the study
  • Ensure sites are inspection-ready at all times by ensuring site staff have completed and documented all required trainings, as well as train/support/advise PI and site staff on study-related matters, including RbQM principles.


What we look for in Clinical Research Associates

Requirements vary, depending on the sponsor you will be working for, but generally you’ll need to be an experienced Clinical Research Associate already.

We look for people who are not only skilled at the technical aspects of site monitoring, but can also contribute to broader study design and management.

And for every CRA role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this role:

  • Bachelor degree or above, major in pharmacy or health science related background.
  • Excellent knowledge of ICH-GCP and basic knowledge of GMP/GDP
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management
  • At least 1.5 years of experience in the role of CRA including on-site monitoring.
  • Excellent command of English (both written and spoken).
  • Good negotiation, collaboration and interpersonal skills

Not quite the CRA role for you?

Don’t worry we need CRAs for different locations, sponsors, and therapeutic areas, and at entry, mid and senior levels.

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