Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team-focused environment as you explore unique career opportunities?If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp as a Clinical Trial Data Analyst.In this role, you will be assigned a portfolio of clinical studies and you will be responsible for ensuring that each month these studies laboratory data is on track by consulting an internal dashboard. Specifically, that the laboratory specimens are collected per protocol and that they are being processed and resulted as expected. If they are not, your role will be to investigate why that is not happening and share those insights with the Global Study Managers as to how to rectify and prevent those issues. The Global Study Managers are accountable for the entire protocol.Additionally, you will be responsible for putting in place customized, study specific monitoring packages of low to moderate complexity for studies 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 Clinical Trial Data Analyst must be in compliance with the Central Labs Global Project Management strategy and deliver outstanding performance and customer satisfaction.In more details, you will…
Accountable for the monitoring and reporting of clinical study laboratory metrics on both a monthly and/or ad hoc basis.
Ability to extract information from multiple data sources, converting the raw data into meaningful and actionable insights, and presenting key findings to your stakeholders (the Global Study Manager (aka the study Project Manager) and the Study Design Lead (aka the study Technical Writer).
Utilizing analytics/visualizations to review study laboratory data for your assigned studies to identify issues and to ensure risks are proactively addressed.
Ensure regular communication with your key internal stakeholders.
Participating actively to LabCorp development through continuous process improvements.
Able to act efficiently in an environment with dynamic timelines and priorities.
Participate in functional meetings ((e.g. LabCorp Learning Forums)) and provide input, keeping processes up to date.
Comply with Central Labs Global Project Management strategy.
Support a culture of continuous improvement, quality and productivity.
Other duties as assigned.
Thrive personally and professionally at LabcorpWorking at Labcorp, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s life.In addition, Labcorp offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.What we’re looking forClinical Trial Data Analysts are most successful at Labcorp with:Minimum Experience Required:
3-5 years of related experience (Education can substitute for work experience)
Demonstrated advanced level of Excel knowledge
Minimum Education Required:
University degree (minimum Bachelor level, data or scientific fields preferred)
Get to know LabcorpAt Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.Here, you can join our more than 60,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.Pay Range: $45,594 - $87,819Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable. For more detailed information, please click here (https://cdn.phenompeople.com/CareerConnectResources/COVAGLOBAL/documents/Labcorp-Benefits-TheWayWeLive-1659629596356.pdf) .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.For more information about how we collect and store your personal data, please see our Privacy Statement (https://www.labcorp.com/hipaa-privacy/web-privacy-policy) .