Clinical Site Manager (CRA)
Parexcel
Argentina
hace 2 días

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.

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.

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 requirementsYour Key Accountabilities :

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 :

Monitoring patient safety on-site and addressing any violations in a timely manner

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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