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Clinical Site Manager I / CRA I

China - Shanghai - Home Based Date posted 12/04/2018 Job ID 49494BR

At PAREXEL, we believe that the power to work independently and intelligently should be yours every day. Your ability to understand our clients’ needs and achieve quality results is critical to our reputation as one of the best clinical research organizations (CROs) in the world.

As a Clinical Site Manager (CRA) within PAREXEL's Global Monitoring Operations Group, we support you with leading-edge technology, the highest caliber team members, and managers who know your strengths. If you're looking for flexibility and work-life balance, we're here to listen and help you move forward with your individual career path.

  • Full Time
  • Level: Mid
  • Travel: Yes
  • Glassdoor Rating 3.5

Success Profile

What makes a successful Clinical Site Manager at PAREXEL? Check out the top traits we’re looking for and see if you have the right mix. Additional related traits listed below.

  • Innovative

    9
  • Problem-solver

    9
  • Presenter

    8
  • Technologically savvy

    10
  • Confident

    6
  • Independent

    5
  • organized
  • analytical
  • goal-oriented
  • quick-thinking
  • motivational
  • team player
  • managerial
  • curious

"One thing I enjoy about my job is when I see patients feel better with the new treatments; that is very gratifying. I always think about the pleasure our work can give patients and their loved ones."

- Wagner – Associate Manager, Clinical Operations
 

Rewards

  • 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

    Opportunity to work on a wide range of therapeutic areas and medical devices.

  • Compensation

    Competitive salaries and bonus structure based on individual metrics.

Responsibilities

PAREXEL has launched a new clinical operating model to drive effectiveness, reduce hand-offs and increase employee, client and site satisfaction. Within this model, the Clinical Site Manager (CSM), formerly the Clinical Research Associate (CRA), serves as the clinical sites’ direct point of contact. The CSM role offers the opportunity to go beyond the role of a typical clinical monitor. CSMs are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. This includes addressing and resolving site issues and questions. You will also manage site quality and delivery from site identification through to close-out.

As a CSM, PAREXEL will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work will be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas, and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, please apply to learn more.

Your Key Accountabilities:
  • Act as PAREXEL’s sole contact with assigned clinical sites
  • Use your trial management expertise to oversee overall integrity of the study and problem-solving skills to promote positive working relationships with the site and staff
  • Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites; generate visit/contact report
  • Review the performance of the trial at designated sites, ensuring the rights and well-being of human subjects are protected and are in accordance with protocol
  • Evaluate the quality and integrity of the reported data, site efficacy, and drug accountability
  • Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines Ensure compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s)
  • Monitor completeness and quality of Regulatory Documentation and perform site document verification

Qualifications

Your Skillset:
  • Previous relevant work experience preferred
  • Educated to degree level (biological science, pharmacy or other health related discipline)
  • Demonstrates strong interpersonal, written, and verbal communication skills within a matrixed team
  • Ability to work in a self-driven capacity, with a sense of urgency and limited need for oversight
  • Client focused approach to work; flexible attitude with respect to work assignments and new learning
  • Ability to manage multiple tasks, to evaluate a variety of unpredictable scenarios, and achieve project timelines; apply understanding of study protocol(s)
  • Work ethically and honestly to promote the development of life changing treatments for patients
  • Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word
Our Offer:

Join the best minds in the industry and leverage your expertise to help advance treatments into the hands of those who need them most. This role is an excellent opportunity to enhance your skills and take the lead on client projects.

We look forward to speaking with you and determining how PAREXEL fits into your career journey!

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