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ICON plc logo
ICON plc

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Site Partner II – Senior Site Partner

Affiliate ManagerAffiliate MarketingFull TimeRemoteSeniorTeam 10,001+Since 1990H1B No SponsorCompany SiteLinkedIn

Location

North Carolina + 1 moreAll locations: North Carolina | Tennessee

Posted

93 days ago

Salary

0

Seniority

Senior

Bachelor Degree0.3 yrs expEnglishGoogle Cloud Platform

Job Description

Site Partner II – Senior Site Partner

ICON plc

• Accountable for the proficient and proactive co-ordination of all necessary activities required to achieve timely site activations and maintenance tasks for any given site(s) across a single or multiple studies. • Act as site liaison and escalation point of contact; proactively resolving issues to ensure the site receives a positive customer experience. • Ensure CDP and Site Activation approval dates are forecast and planned accurately in ICON’s systems, documenting all risks to delivery with mitigations taken, as they occur. • Collect and collate site Critical Package Documents (CDPs) for review and approval prior to site activation in accordance all requirements, ensuring the highest quality, accuracy and completeness of site and country documentation is obtained in the TMF. • Expert knowledge of ICON SOPs/WPs, ICH/GCP and applicable country regulations/guidelines and ICON systems. • Work with key stakeholders to optimize performance and collaborate to ensure successful project outcomes. • Drive CDP and site activation timelines and ensure they are reflected accurately in ICON’s systems and are achieved; proactively follow through for achievement to plan; provide risk assessment and contingency plans at a site level, to mitigate impact if forecasted timelines are at risk; escalate issues as soon as identified. • Ensure timely submission of protocol and study documents/safety reports for local ethics/IRB approval according to local requirements. • Provide support, with the preparation and supply of site documentation required for regulatory submissions. • Accurate site and country adaptation and customizations of Patient Informed Consents. • Develop and update training documentation and conduct group trainings in the assigned areas of expertise.

Job Requirements

  • Bachelor's Degree
  • 0-3 years of experience in a Clinical Research environment
  • Good communication skills
  • Good Judgment & Decision Making
  • Proficient computer knowledge.
  • Proficiency in English language is mandatory.
  • Bachelor's Degree
  • 6-9 years of experience in a Clinical Research environment
  • Excellent communication skills
  • Good Judgment & Decision Making
  • Proficient computer knowledge.
  • Proficiency in English language is mandatory.

Benefits

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize 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.

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