Regional Study Coordinator

Labcorp is seeking a remote Regional Study Coordinator (1-year contract) to join our team in United Kingdom!

Work schedule:

Monday – Friday

• Manage the day-to-day activities of a clinical trial at a regional level. RSCs manage multiple studies and the responsibilities for each include:
• Collaborate with the Global Study Manager for all local study related aspects. Specifically, study set up and closure; ordering of study start up supplies, answering CRA questions regarding country specific regulations, etc.
• Act as regional liaison between Global Study Manager and various CLS departments involved in the study.
• Act as a regional liaison between assigned client representatives (e.g., Clinical Research Associates (CRAs) or Site Monitors) and Labcorp
  
  CLS internal departments and teams.
• Monitor, track and provide resolution to all local study issues; especially logistic issues and/or delays in receipt of study supplies, all the while keeping the Global Study Manager in the communication loop.
• Clean the laboratory database; e.g., a lab sample has been placed on hold and is not being analyzed, determine why it is not being processed and then resolve the issue.
• Deliver outstanding customer service and timely responsiveness to ensure client satisfaction, which requires a clear understanding of study design and major budget drivers.
• Work in a matrix environment where some task assignments are being channeled down to be dealt with by RSCs while other task assignments will need to be delegated by Regional Study Coordinators to other functional groups.

• Bachelor degree
• 1 or more years of Clinical Project management experience within clinical studies
• 1 or more years of experience in Central Lab services
• Fluency in English

• University degree
• 1 or more years of experience in external client communication or stakeholder management

• Excellent communication and organization skills
• Demonstrated time management skills
• Dedicated to teamwork
• Ability to plan and prioritize
• Thrive in a fast-paced environment

This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. It is remotely based and a temporary 1-year contract.

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.

Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

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