Data Manager

Labcorp; Indianapolis (IN); Presencial; USD 65.000 - 72.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical

Dental

Vision

401(k)

Paid Time Off

Tuition Reimbursement

Employee Stock Purchase Plan

Descripción de la vacante

Labcorp is seeking a data management professional to act as the primary contact for clinical studies, guiding start-up, data transfer specifications, and data quality improvement. You will work with clients and internal teams to ensure accurate data integration and timely study milestones.

Responsibilities include coordinating data management activities, supporting end-to-end data lock, and contributing to process improvements in a global, cross-functional environment.

Formación

• Experience in data management for clinical studies.
• Strong written and verbal communication across cross-functional teams.
• Ability to define workflows and ensure data quality.

Responsabilidades

• Act as the primary data management contact for assigned clinical studies.
• Lead start-up activities and develop data transfer strategies.
• Collaborate with clients to finalize Data Transfer Specifications (DTS).
• Provide guidance to optimize data quality, reporting, and transfer processes.
• Coordinate data management activities supporting end-to-end data lock processes.

Conocimientos

Data Management

Clinical Trials

Communication

Microsoft Office

Data Transfer

Educación

BS/BA or equivalent

Associate degree with 4 years data management experience

Herramientas

Microsoft Office

Descripción del empleo

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 a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives. Labcorp is a global leader in diagnostic testing and drug development solutions, helping healthcare providers, researchers, and patients make informed decisions that advance care. Join us in our mission to improve health and improve lives.

Work Schedule Monday – Friday, 8am – 5pm EST

Job Responsibilities

• Act as the primary data management contact for assigned clinical studies, partnering with clients from study start-up through database lock and study completion.
• Lead study start-up activities, including review of study requirements, establishment of documentation, and development of data transfer strategies.
• Collaborate with clients to define, develop, and finalize Data Transfer Specifications (DTS), ensuring accurate and efficient data integration.
• Provide expert guidance and recommendations to optimize data quality, reporting, and data transfer processes.
• Serve as a key liaison between Clinical Data Management and cross-functional teams including Project Management, Medical Affairs, Specimen Management, and other operational groups.
• Design, develop, test, and maintain data transfer formats and processes in accordance with client requirements, internal standards, and regulatory expectations.
• Oversee the delivery and validation of data transfers, ensuring quality, accuracy, and timely execution.
• Provide ongoing study support, including troubleshooting data issues, managing change requests, addressing client queries, and implementing study modifications.
• Coordinate data management activities supporting end-to-end data lock processes and study milestones.
• Participate in client meetings, audits, inspections, bid defenses, and other customer-facing activities as a Clinical Data Management representative.
• Support the evaluation and implementation of new client services, process improvements, and operational efficiencies.
• Maintain complete and audit-ready study documentation, records, and metrics in compliance with applicable procedures and regulatory requirements.
• Track study portfolios, workload, and productivity metrics to ensure effective delivery across assigned projects.
• Contribute to a collaborative team environment by sharing expertise, supporting colleagues, and providing backup coverage when needed.
• Continuously develop technical and industry knowledge through corporate, departmental, and sponsor‑specific training programs.

Minimum Qualifications

• High School Diploma

Preferred Qualifications

• BS/BA four-year degree/equivalent and 2-year equivalent Data Management experience or 2-year Associate degree/equivalent with 4 years Data Management experience and/or Leadership experience

Additional Job Standards

• Strong organizational, planning and critical-thinking skills.
• Well-polished, inclusive, and engaging communication skills (written and verbal).
• Strong negotiation skills to facilitate, guide, influence, and produce a unified approach within a global, cross-functional environment.
• Ability to handle multiple tasks in a timely and professional manner under demanding conditions.
• Ability to use standard Microsoft suite of software products.
• Conversant with databases and database terminology.
• Strong technical aptitude.
• Customer Service experience.
• Data Management and/or Clinical Trials experience.

Application Window

October 27, 2026 – November 3, 2026

Pay Range

$65,000 - $72,000 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.

Benefits

• Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.
• Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.

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 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.