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:
1. Act as regional liaison between Global Study Manager and various LCLS departments involved in the study.
2. Act 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.
3. Close 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.
4. Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead.
5. Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial.
6. Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development.
7. Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop.
8. Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed.
9. Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan
10. Demonstrate 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.
11. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date.
12. Comply with LCLS Global Project Management strategy.
13. Support a culture of continuous improvement, quality and productivity.
14. Other 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.

Qualification:

Bachelor Degree in relevant fields.

Relevant professional / internship experience in clinical research or pharmaceutical industry will be an advantage

Business level of English

Ability to use computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook)

Strong interpersonal skills

Influence and negotiation skills

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

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility.

For more information about how we collect and store your personal data, please see our Privacy Statement.