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Seasonal Labcorp Clinical Trials information

What is a seasonal Labcorp Clinical Trials job?

Seasonal Labcorp Clinical Trials jobs are temporary positions offered by Labcorp to support clinical research studies during peak periods. Employees in these roles may assist with tasks such as data entry, sample processing, patient recruitment, and administrative duties related to clinical trials. These jobs are ideal for individuals seeking short-term employment or experience in the clinical research field. Seasonal positions typically last for a few months and may offer opportunities to learn about the clinical trial process and work alongside experienced professionals.

What skills and qualifications are needed for a seasonal Labcorp Clinical Trials job?

To thrive as a Seasonal Labcorp Clinical Trials employee, you generally need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Knowledge of laboratory equipment, data management systems, and compliance with regulatory standards such as Good Clinical Practice (GCP) is often required. Strong organizational skills, clear communication, and the ability to work efficiently in a team-oriented and fast-paced environment are highly valued. These skills and qualities are critical to ensure precise data collection, patient safety, and the overall success of clinical research projects.

What challenges are common in a seasonal Labcorp Clinical Trials role, and how can I prepare for them?

In a seasonal role with Labcorp Clinical Trials, common challenges include adapting quickly to fast-paced workflows, managing large volumes of samples or data during peak periods, and learning new protocols efficiently. Since the work is project-based and timelines can be tight, strong organizational and communication skills are essential. Being proactive in seeking guidance and collaborating closely with your team will help you succeed and make a positive impact, even during a short-term assignment.
More about Seasonal Labcorp Clinical Trials jobs

What cities are hiring for Seasonal Labcorp Clinical Trials jobs?

Cities with the most Seasonal Labcorp Clinical Trials job openings:

What are the most commonly searched types of Labcorp Clinical Trials jobs?

The most popular types of Labcorp Clinical Trials jobs are:

What states have the most Seasonal Labcorp Clinical Trials jobs?

States with the most job openings for Seasonal Labcorp Clinical Trials jobs include:

What job categories do people searching Seasonal Labcorp Clinical Trials jobs look for?

The top searched job categories for Seasonal Labcorp Clinical Trials jobs are:

Seasonal Labcorp Clinical Trials jobs near you
Infographic showing various Seasonal Labcorp Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Sr. Manager IVD Manufacturing and Operations CDx

Labcorp

Morrisville, NC • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 23 days ago

Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,145 frontline employees who took The Breakroom Quiz

96th of 120 rated laboratories

Job description

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives.
Labcorp is seeking a Senior Manager IVD Manufacturing and Operations CDx to join our team in Morrisville, NC!
Job Responsibilities:
The Senior Manager is a hands-on CDx Manufacturing and Operations leader and will grow a small but critical Companion Diagnostics (CDx) manufacturing function. This role will work alongside an existing team member and will be directly responsible for the development, manufacturing, and commercialization of IVD companion diagnostic kits from clinical trials through global launch (US, EU, and RoW). This position requires someone who can execute day-to-day technical work while also providing vision and leadership to evolve processes, infrastructure, and capabilities as the CDx portfolio expands. Lead manufacturing operations and ensure facility readiness in direct support of the development, manufacturing, and commercialization of IVD/CDx kits used in clinical trials and commercial launch for US, EU, and ROW markets which includes:
  • Ensure manufacturing operations comply with applicable regulations and standards, including FDA, IVDR, ISO 13485, and global IVD requirements
  • Perform and oversee assay transfer, manufacturing process development, validation, and scale-up activities. Own day-to-day manufacturing execution, troubleshooting, documentation, and lifecycle management activities in a small-team environment
  • Manufacturing of kits and preparation of final packaging of IVD products and PM activities for shipment to clients and/or Field Service Technicians
  • Coordinating and expediting the flow of materials and assemblies between departments, according to production and shipping schedules or department priorities
  • Partner with cross-functional teams to regulatory support submissions, internal and external audits, and post-market activities
  • Establish metrics and KPIs to track performance, quality, and delivery
  • Be an active member of internal project team, including participating in project-set up activities and team meetings
  • Represent the CDx manufacturing function in internal governance forums
  • Build scalable foundations (processes, documentation, tools) appropriate for a growing organization
  • Training and ensuring competency of manufacturing staff

Minimum Qualifications:
  • Bachelor of Science degree
  • 2 or more years of experience as a supervisor or manager
  • 3 or more years of experience with PeopleSoft, ERP systems, Microsoft Office and FedEx Computer shipping software and hardware systems
  • 5 or more years of experience with IVD regulations and quality systems (FDA, IVDR, ISO 13485)
  • 8 or more years of experience in assay development and kit commercialization

Preferred Qualifications:
  • 5 or more years of experience with supply chain management, production, inventory management, manufacturing or logistics utilizing batch records

Additional Job Standards:
  • Ability to effectively manage teams in a regulated environment
  • Ability to effectively perform organizational, analytical, planning, and computer skills
  • Ability to be effective in verbal and written communication skills
  • Ability to lead cross-functional initiatives and influence others.
  • Ability to work independently and in a team environment with a professional and positive attitude
  • Ability to manage and maintain relationships with internal and external partners with professionalism and manage multiple concurrent studies each at a different stage
  • Ability to manage processes with high quality and master new techniques in an accelerated manner
  • Ability to work effectively and efficiently under pressure to organize work and meet scheduled deadlines
  • Ability to sit, stand, and walk for extended periods
  • Ability to pull, push, or lift of heavy objects up to 75lbs.

At Labcorp, you can expect the following:
  • Innovative Environment: Join a leading healthcare organization committed to driving innovation through strategic investments to help improve health and improve lives.
  • Global Impact: Contribute to the future of healthcare by investing in pioneering companies that can transform patient care.
  • Collaborative Culture: Work in a dynamic, inclusive environment that values diverse perspectives and fosters collaboration.

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. For more detailed information, please click here.
  • Relocation assistance available.

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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