Skip to main content

This job has expired

Site Feasibility Liaison

Employer
Parexel
Location
Hungary
Salary
Competitive
Start date
14 Jan 2022
Closing date
26 Jan 2022

View more

Discipline
Clinical Research
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Job Description

Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do.We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability. Join us and you'll make a profound difference in millions of lives. We're not just the people with expertise, we're the peopleWith Heart®.

Parexel has an exciting opportunity for an experienced Site Feasibility Liaison (SFL) this is a critical role for the delivery of Parexel studies and setting up a trial for success. The SFL must demonstrate strong communication skills to build effective relationships with Investigators and research sites and will champion Parexel within their region.

The SLF will be a local clinical expert to represent their country/region and will be the advocate for their region to ensure it is included in the Parexel portfolio and support new business opportunities by helping to gather critical data to support client meetings or deliverables. An expert in terms of local infrastructure, standards of care, healthcare trends and guidelines. Working in conjunction with site intelligence and site alliance teams, will work to improve the knowledge that we have on clinical research teams and facilities including owning the quality of information within the Investigator Intelligence Platform that pertains to their country, region or therapeutic area.

Key Accountabilities:
  • Responsible for the review draft site lists, communicate with sites to ensure high response rates, co-ordinate CDA collection and query inconsistent/incomplete survey information, provide data-driven recommendations with regards to site selection
  • Conduct phone interviews/follow-up with Investigators or site personnel to discuss standard of care, trends, patient barriers, protocol design considerations
  • Support the central feasibility teams with local insight to support country strategy, protocol development and new business awards. Provide accurate, timely and realistic information
  • Proactively work to understand healthcare re-imbursement, trial infrastructure, patient motivations, patient support groups, site networks, new potential sites/Investigators for consideration in your country, region, therapy area
  • Understand, communicate, and help to mitigate the risks to delivery for your country, region, therapy area
  • Proactively work to ensure accuracy of critical information held in the Investigator Intelligence Platform relevant to your country, region or therapy area. Work to build out valuable profile information for key sites to improve efficiency and improve the site experience
  • Actively work with clinical and medical experts in your country to promote collaboration and to facilitate information gathering
  • Work closely with central feasibility counterparts to ensure a common understanding of risk and to promote the consideration of your country or region in future trials
  • Develop and maintain collaborative relationships with Investigators and site personnel
  • Promote a culture of innovation and respect with the patient first and foremost
  • Provide cross boarder support
  • Qualifications

    Knowledge/Skills:
  • Several years Pharmaceutical/CRO Industry experience in Clinical Research
  • Wealth of experience in clinical management/feasibility management of global clinical trials with significant local clinical experience
  • Demonstratable understanding and experience in selecting and starting up clinical trial sites
  • Fluent in English, oral and written
  • Fluent in local language, as applicable
  • Other language skills beneficial
  • Autonomous, driven, takes pride in quality of work, attention to detail
  • Ability to build effective relationships with others (Investigators, research teams)
  • Independent thinker and fast leaner
  • Exceptional analytical and problem-solving skills
  • Effective interpersonal, presentation, oral and written communication skills
  • Capability to work in a matrix environment and to value the importance of teamwork.
  • Ability to manage multiple tasks, to be flexible and to prioritize
  • Strong client focus - sense of urgency to respond to client requests
  • Strong computer skills

  • Education
  • Degree / further degree
  • Scientific/Medical/Nursing background preferred

  • Language Skills
  • Fluent in English, oral and written
  • Fluent in local language, as applicable
  • Other language skills beneficial
  • Why Work at Parexel

    There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

    That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

    How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.

    Company

    parexel

    When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

    How to describe Parexel’s culture in one word: 

    Henry

     

     

    Working With Heart™ - Christina's perspective:

    Working With Heart™ - Christina's perspective:

     

    Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process

    Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

    Company info
    Website
    Telephone
    +44 1895 238000
    Location
    The Quays
    101-105 Oxford Road
    Uxbridge
    Middx
    UB8 1LZ
    United Kingdom

    Get job alerts

    Create a job alert and receive personalised job recommendations straight to your inbox.

    Create alert