Clinical Data Risk & Solutions Analyst (Global Monitor)

BVB Labcorp BV; Mechelen; Remote; EUR 55,000 - 75,000; Full time

Job summary

Labcorp is seeking a remote Clinical Data Risk & Solutions Analyst (Global Monitor) to join our Belgium-based team. The role involves managing a portfolio of studies, identifying risks, developing mitigation plans and writing monitoring instructions for study oversight.

You will ensure study health and compliance with the Global Project Management strategy. Qualified candidates will have a science degree, 3+ years in clinical data analysis or project management, English fluency, and strong

Qualifications

• University degree in science.
• 3+ years of experience in clinical project management or clinical data analysis.
• 1+ years of experience in the life science, healthcare or pharmaceutical industry.
• Fluency in English.

Responsibilities

• Accountable for the monitoring and reporting of clinical study laboratory metrics.
• Extract information from multiple data sources and present key findings to stakeholders.
• Perform risk assessments and propose monitoring solutions to mitigate identified risks.
• Utilize analytics/visualizations to review study laboratory data and identify issues.
• Liaise with Developers to ensure monitoring tools meet client specifications.
• Ensure regular communication with key stakeholders and support Risk Management Plan maintenance.

Skills

Fluency in English

Education

University degree in science

PhD degree in science

Tools

Excel

Job description

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.

Job Description

Labcorp is seeking a remote Clinical Data Risk & Solutions Analyst (Global Monitor) to join our team in Belgium

Labcorp manages one of the largest networks of clinical laboratories in the world. In the Clinical Data Risk & Solutions Analyst (Global Monitor) role, you will be assigned a portfolio of clinical studies. When a new study starts, the Global Monitor works with the internal teams to identify study risks and develop mitigation plans. Global Monitors also look for issues in the study data and suggest actions internally and/or externally to rectify and prevent those issues and maintain study health. Additionally, you will be responsible for putting in place customized, study specific monitoring packages for studies based on study needs or in which clients are requesting additional oversight by Labcorp to ensure all their samples will be processed correctly. To do this, you will need to understand which laboratory samples are at risk for not being resulted on time, to choose which of our monitoring offerings is best suited for the study needs, and then to write clear monitoring instructions that will be handed off to another part of the team. Overall, the Global Monitor must be in compliance with the CCLS Global Project Management strategy and deliver outstanding performance and customer satisfaction.

Job Responsibilities

• Accountable for the monitoring and reporting of clinical study laboratory metrics.
• Ability to extract information from multiple data sources, converting the raw data into meaningful and actionable insights, and presenting key findings to all stakeholders (internal and external).
• Performing risk assessments on low complexity studies in coordination with the Global Study Manager and the Study Design Lead prior to study start and proposing monitoring solutions to mitigate the identified risks.
• Utilizing analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.
• Liaise with Developers to ensure development of monitoring tools are completed to the client’s specifications
• Ensure regular communication with your key stakeholders.
• Support Risk Management Plan creation and ongoing maintenance through monitoring and analysis
• Participate actively to Labcorp development through continuous process improvements.
• Be able to act efficiently in an environment with dynamic timelines and priorities.
• Participate in functional meetings and provide input, keeping processes up to date.
• Comply with internal strategy.
• Support a culture of continuous improvement, quality and productivity.

Minimum Qualifications

• University degree in science
• 3 or more years of experience in clinical project management or clinical data analysis
• 1 or more years of experience in the life science, healthcare or pharmaceutical industry

Preferred Qualifications

• PhD degree in science
• 3 or more years of experience in Excel
• 1 or more years of experience in client management

Additional Job Standards

• Fluency in English
• Curious, data driven analytical thinker
• High quality standards, attention to detail
• Strong motivation, flexibility and creativity
• Big picture thinker who suggests changes to process, identifies risks and potential opportunities for data improvement
• Strong problem-solving and customer service skills
• Comfort with ambiguity and fast switching across studies/portfolios as priorities change
• Able to operate with minimal guidance while owning deliverables end-to-end
• Proven ability to effectively communicate ideas/concepts and to motivate/influence others to accomplish challenging shared goals and objectives.
• Dedication for learning and self-improvement
• Robust self-organization; at-ease with managing conflicting priorities
• Ability to create and motivate a team around project deliverables

Labcorp is proud to be an Equal Opportunity Employer

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 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. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care.