Global Study Manager - 1 year contract

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

Labcorp is seeking a remote Global Study Manager (1year contract) to join our team in Poland.

Work schedule: Monday - Friday

Job Responsibilities:

• Key contact for clients; Liaison between Clients, CRO, and Labcorp

• Displays leadership to ensure successful interactions between LabCorp study team members needed to provide seamless study delivery to the client.

• Provides project management oversight; focusing on key client deliverables through budget, risk, and milestone management.

• Facilitates communications between Client and extended LabCorp study team, including Study Design Lead and Regional Study Coordinator.

• Performs review of SOW to ensure quality implementation of client specifics and requirements.

• Manages a portfolio of global and local studies with varying complexity.

• Acts as an ambassador on behalf of the client within LabCorp Drug Development CLS and across LabCorp business units; exemplifies the concept of Signature Client Service through outstanding, personalized customer service skills

• Ensures that all customer expectations are documented and acted upon in compliance with regulatory requirements

• Demonstrates through appropriate self-organization the ability to manage conflicting priorities and to make difficult decisions

• Able to act efficiently in an environment with dynamic timelines and priorities

• Accountable for the implementation, monitoring and reporting of performance metrics

• Actively participates in LabCorp CLS development through continuous process improvement, quality and productivity

• Work with appropriate internal and external personnel to understand the culture and pipeline of assigned clients

• Demonstrates strong interpersonal and communication skills that will build strong internal and external relationships to ensure deliverables are on time and within budget

• Displays appropriate self-organization and ability to manage conflicting priorities

• Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date

• Comply with CLS Global Project Management strategy

• Support a culture of continuous improvement, quality and productivity

• Other duties as assigned

Minimum Qualifications:

• Bachelor degree

• 2 or more years of experience in clinical project management

• 2 or more years of experience in clinical trial industry

Preferred Qualifications:

• Master degree or University degree

Additional Job Standards:

• 1 or more years of experience in driving projects, preferably with global teams

• 2 or more years experience in client facing (internal and external stakeholder) and stakeholder management.

• Ability to manage client relationships, deal with escalations, and provide exceptional customer service and support

• Strong communication and problem solving ability

Get ready to redefine what’s possible and discover your extraordinary  potential. Here at Labcorp, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. 

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

The Company - LabCorp

As one of the world's largest and most comprehensive drug development services companies, LabCorp has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.

The Position: Global Study Manager

This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. In this role you will support a key client account in leading pharma.

The Global Study Manager must prove to be knowledgeable and experienced in project management techniques related to clinical trials. The Global Study Manager is responsible for key client deliverables including budget, risk, and milestone management. Global Study Managers must demonstrate leadership across the LabCorp study team, keeping a collaborative attitude and fostering excellent communication within the team. Global Study Manager must be able to combine a strong understanding of client protocol specifics and study feasibility, to ensure successful study management and provision of outstanding customer service.

You can work fully remote in this role.

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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