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Site Engagement Liaison

ICON

United Kingdom

Remote

GBP 35,000 - 65,000

Yesterday
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Job summary

Join an innovative biopharmaceutical company as a Site Engagement Liaison, where you will be the key contact for investigative sites throughout the study lifecycle. This role involves managing site start-up activities, building strong relationships with investigators, and ensuring compliance with regulatory standards. You will collaborate with various stakeholders to optimize site selection and maintain effective communication throughout the study. With a commitment to diversity and inclusion, this forward-thinking organization offers a dynamic work environment and a range of competitive benefits to support your well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualifications

  • 5+ years experience in site management with a focus on activation and conduct.
  • Knowledge of Good Clinical Practice and regulatory requirements.

Responsibilities

  • Accountable for site start-up, activation, and study conduct.
  • Act as the operational point of contact for site-level inquiries.

Skills

Site Management

Communication Skills

Regulatory Knowledge

Cross-functional Relationship Management

Problem-solving Skills

Education

Bachelor’s degree or RN in a related field

5 years experience in site management

Tools

EDC

Shared Investigator Platform

Job description

Title - Site Engagement Liaison

Location - Must be based in the UK and open to reduced nationwide travel

Sponsor dedicated

As a Site Care Partner you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


Working fully embedded within an innovative biopharmaceutical company, you will be the main point of contact for investigative sites throughout a study life cycle; accountable for site start-up activities through activation; accountable for building and retaining investigator site relationships and providing support from site recommendation through the lifecycle of studies.

What you will be doing:

Accountable for site start-up and activation:

  • Deploy GSSO site strategies by qualifying and activating assigned sites.
  • Supports processes to optimize country & site selection activities including review and assessment of the draft potential site list & provide PTA output for site selection.
  • Collaborate with key stakeholders providing country/regional level input to country outreach surveys including protocol feasibility, country SOC and medical practices (as applicable) under supervision.
  • Maintain a thorough knowledge of assigned protocols.
  • Conduct study start up activities at the site level including but not limited to PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation.

Accountable for study conduct and close-out:

  • Act as operational point of contact for all site-level questions, liaising with and escalating to appropriate teams to respond and resolve questions.
  • Review Site Monitoring Reports.
  • Support the site with revision and submission of ICD documents (and amendments).
  • Working with other roles, maintain system management (e.g., EDC, Shared Investigator Platform, Site Profile and other systems as applicable) at site level ensuring alignment across platforms.
  • During the conduct of the study, the Site Management Organization Assessment is reviewed with the site, when applicable, on an annual basis following site initiation and updated as needed under DCSO/ Senior SCP supervision.

Responsible for proactively providing local intelligence:

  • Provide input into site recommendations via intimate understanding of country/region, sites, processes and practices, and associated site performance metrics.
  • Provide support to the Study Operations Manager/Global Study Manager to define local requirements for the importation/exportation processes of the investigational medical product and ancillary supplies.

You must have the following:

  • Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience (estimate at least 5 years experience).
  • Proficiency in local language preferred. English is required.
  • Demonstrated experience in site management with prior experience as a site monitor.
  • Demonstrated experience in start up activities through to site activation.
  • Demonstrated experience in conduct and close out activities.
  • Demonstrated knowledge of quality and regulatory requirements in applicable countries.
  • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
  • Must demonstrate good computer skills and be able to embrace new technologies.
  • Good communication, presentation and interpersonal skills.
  • Ability to manage required travel of up to 75% on a regular basis.
  • Demonstrated ability to manage cross functional relationships.
  • Identifies and builds effective relationships with investigator site staff and other stakeholders.
  • Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements.
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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