Site Monitor II

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Substantial Site Management experience or equivalent experience in clinical research, particularly in oncology trials., Understanding of clinical trials methodology and terminology., Excellent presentation skills and a client-focused approach., Ability to prioritize multiple tasks and work independently while seeking guidance when necessary..

Key responsibilities:

  • Act as the direct point of contact for clinical sites, managing site quality and delivery from identification through close-out.
  • Build relationships with investigators and site staff, facilitating access to study systems and ensuring compliance with training requirements.
  • Update Clinical Trial Management Systems (CTMS) regularly, ensuring high-quality data entry compliance and managing relevant documents for the Trial Master File (TMF).
  • Work collaboratively with team members to meet project goals and develop strategies for efficient project planning and completion.

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Parexel XLarge http://www.parexel.com
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Job description

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel are currently recruiting for an experienced CRA to cover sites across Denmark.

In this position you will be an invaluable resource being the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out.

The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to initiation, the development of a robust patient recruitment strategy, setting up a system, assessing compliance with regulations and the site’s capability to comply with the study needs and recruitment expectations, and problem solving to address and resolve site issues.

Some specifics about this advertised role

  • Build relationships with investigators and site staff.
  • Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.
  • Evaluate if on-site staff assignment is still accurate and determine and implement corrective actions & follow-up, if necessary / relevant.
  • Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required.
  • Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis, including performing regular reviews of site level data in clinical systems (e.g. CTMS, EDC, IVRS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

What we are looking for in this role

For every 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 advertised role.

  • Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Specifically within oncology trials.
  • Able to take initiative and work independently, and to proactively seek guidance when necessary.
  • Excellent presentation skills.
  • Client focused approach to work.
  • Ability to interact professionally within a client organization.
  • Flexible attitude with respect to work assignments and new learning.
  • Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Analytical Skills
  • Communication
  • Time Management
  • Physical Flexibility
  • Problem Solving

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