Regional Study Coordinator
Regional Study Coordinator
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Job Description
Job Summary:
The Regional Study Coordinator (RSC) is responsible for the successful delivery of all operations of a clinical study in their specific area of the world. The RSC acts as the appointed Liaison between Global Project Management Client Representatives and other LCLS departments involved in the clinical study to ensure the successful management of regional study responsibilities. The Regional Study Coordinator may communication with the Client when a task is being delegated by the Global Study Manager. Regular communication is essential with the appointed Global Study Manager who is accountable for the entire protocol. This position must be in compliance with the LCLS Global Project Management strategy and deliver outstanding customer satisfaction and performance.
Essential Job Duties:
as regional liaison between Global Study Manager and various LCLS departments involved in the study.
as regional liaison between assigned Client representatives (eg. CRA Site Monitors) and the corresponding local LCLS platform; occasionally the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact.
collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages from set-up to closure.
the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead.
a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial.
day-to-day local study related activities especially logistics monitoring and study supplies keeping the Global Study Manager informed of any study development.
track and provide resolution to all local study issues keeping the Global Study Manager in the communication loop.
for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed.
with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan
ability to work in a matrix environment where task assignments can be channeled down to be completed by Regional Study Coordinators while other task assignments will need to be delegated to other functional groups; demonstrate flexibility in handling both categories of tasks.
in functional meetings (eg. CLFs) and provide input keeping processes up to date.
with LCLS Global Project Management strategy.
a culture of continuous improvement quality and productivity.
duties as assigned.
The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above.
Experience:
Minimum Required:
Demonstrated ability to plan and prioritize.
Demonstrated communication and organizational skills.
Demonstrated attention to detail.
Proven ability to excel in a fast-paced environment.
Proven teamwork
Proven experience and knowledge of processes and tools used in department.
Demonstrated ability to liaise with internal departments.
Demonstrated ability to facilitate meetings.
Demonstrated participation in process improvement initiatives.
2 years customer service experience preferable in pharmaceutical industry (Education may be substituted for experience)
Education/Qualifications/Certifications:
Minimum Required:
Bachelor or Master degree in relevant fields
Ability to use computer and office software applications (e.g. Microsoft Word Excel MS-Access and Outlook)
Strong interpersonal skills
Strong in English
Influence and negotiation skills
Labcorp is proud to be an Equal Opportunity Employer:
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.
We encourage all to apply
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Required Experience:
IC
Employment Type
Full-Time
