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Clinical Site Manager (CRA)

Argentina - Any Region - Home Based Date posted 11/02/2018 Job ID 44909BR

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 provides monitors with world class technology, training resources, and limited protocol load. You will also be rewarded for your hard work through our CRA bonus incentive program and career advancement opportunities. Our Clinical Site Managers are responsible for managing all site activities resulting in less on site visit requirements

Your Key Accountabilities:

  • Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
  • Act as PAREXEL's direct contact with assigned clinical sites, and use judgment to assess and ensure overall integrity of study implementation, as well as adherence to study protocol
  • Conduct qualification visits (QV), site initiation visits (SIV) and monitoring visits (MV) at assigned clinical sites
  • Good knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Function as a mentor and role model for other CRA team members
  • Manage clinical monitoring activities, including:
    • Arranging on-site visits and logistics
    • Establishment of a site recruitment plan in collaboration with site staff during QV
    • Monitoring completeness and quality of Regulatory Documentation
    • Performing site documentation verification
    • Data collection and drug accountability in accordance with ICH GCP guideline
Monitoring patient safety on-site and addressing any violations in a timely manner

Qualifications

Your Skillset:
  • monitoring experience in clinical research
  • Educated to degree level (biological science, pharmacy or other health related discipline)
  • Strong working knowledge of EDC systems and IVRS
  • Experience of CTMS preferred
  • Competent in written and oral English and Spanish
Our Offer:

We offer you a fascinating and diversified insight into PAREXEL and an exciting journey through the world of clinical research.

You can expect to work with a successful, highly-qualified and dynamic team as you develop your individual scientific profile. You can also look forward to a flexible working environment and a pleasant atmosphere.

If you are ready to join PAREXEL’s Journey, please apply!

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