E.O.N Worldwide

E.O.N Worldwide

Site Activation Manager

Durham, North Carolina

Sponsorship not specified$86k-$170kDetected 15 days ago
GCPProject ManagementBusiness DevelopmentClinical TrialsLeadershipCommunicationCollaboration

About the role

  • Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers.
  • We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.
  • What the Site Activation Manager does at Worldwide Clinical Trials The Site Activation Manager is accountable for site activation project management and delivery activities within the Oncology therapeutic area.

Responsibilities

  • Manage the accurate tracking, analysis, and reporting of site activation progress and metrics.
  • Partner with project teams to support feasibility, site qualification, selection, and regulatory activities as needed.
  • Develop and maintain site activation project plans and support risk assessment and issue resolution.
  • Drive continuous improvement through SOP development, best practices, metrics, and departmental initiatives.
  • Contribute to business development activities, including proposal development and bid defense support.
  • Demonstrated ability to collaborate across the business

Requirements

  • A minimum four-year degree or nursing degree is required
  • Minimum of 4 years CRO experience in Study Start-Up with country lead or manager experience required
  • Promotion to the next level is not automatic based on years of experience.

Compensation

  • will fall within the provided range, and it not a guarantee of exact salary.
  • The final salary will be determined based on relevant experience, performance, education, and internal equity.
  • In addition to base salary, we offer a competitive benefits package depending on location.
  • We ensure pay equity and transparency and comply with all applicable labor laws.
  • Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
  • The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):

Company info

  • We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
  • We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
  • Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
  • Why Worldwide
  • We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe.
  • It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
  • We believe everyone plays an important role in making a world of difference for patients and their caregivers.
  • From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed.
  • We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.
  • What the Site Activation Manager does at Worldwide Clinical Trials
  • The Site Activation Manager is accountable for site activation project management and delivery activities within the Oncology therapeutic area.
  • include coordination, collaboration, and oversight of site identification and central and local ECs (for NA countries only) activities, progression of essential documents collection, monitoring of investigator and site contracts status, and any other country and/or study-specific site activation tasks necessary for Site Activation in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs).
  • May also include pre-award support by providing site activation-related input into the proposal text and budget items.
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