
10,000+ employees
🏥 Healthcare
💊 Pharmaceuticals
🧬 Biotechnology
💰 $2G Post-IPO Debt - LabCorp on 2024-09
Healthcare • Pharmaceuticals • Biotechnology
Labcorp is a global leader in laboratory services, diagnostics, and drug development. The company provides testing, data and scientific insights to doctors, hospitals, pharmaceutical companies, researchers and patients, reaching more than 160 million patients annually. Labcorp operates a large global laboratory footprint with roughly 71,000 employees across 100+ countries and invests in advanced technologies (including AI and digital solutions) to accelerate drug development, support precision medicines (such as cell and gene therapies and oncology diagnostics), and inform clinical decision-making.
🔥 40 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
🏥 Healthcare
💊 Pharmaceuticals
🧬 Biotechnology
💰 $2G Post-IPO Debt - LabCorp on 2024-09
Healthcare • Pharmaceuticals • Biotechnology
Labcorp is a global leader in laboratory services, diagnostics, and drug development. The company provides testing, data and scientific insights to doctors, hospitals, pharmaceutical companies, researchers and patients, reaching more than 160 million patients annually. Labcorp operates a large global laboratory footprint with roughly 71,000 employees across 100+ countries and invests in advanced technologies (including AI and digital solutions) to accelerate drug development, support precision medicines (such as cell and gene therapies and oncology diagnostics), and inform clinical decision-making.
• Interpret sponsor protocol requirements and translate them into a precise, study‑specific database design. • Apply deep technical, therapeutic area, client, and CLS process knowledge to deliver a complete and accurate database design. • Engage regularly with external clients throughout all phases of study design and development. • Partner with internal departments to understand full organizational capabilities and evaluate feasibility of client requests related to study design. • Serve as a consultant on study design decisions, collaborating with the Global Study Manager (GSM) to identify risks and budget implications. • Coordinate internal processes and communications—including feasibility assessments, material transfer agreements, and supply forecasting. • Document all client requirements related to study design and ensure they are fully addressed. • Manage a diverse portfolio of global and local studies with varying levels of complexity.
• High School Diploma • 7 or more years of professional experience working in clinical or preclinical research • 1 or more years of experience working directly with clients and stakeholders • Bachelor’s degree in life sciences (preferred) • 2 or more years of experience working directly with clients and stakeholders (preferred)
• Medical • Dental • Vision • Life • STD/LTD • 401(k) • Paid Time Off (PTO) or Flexible Time Off (FTO) • Tuition Reimbursement • Employee Stock Purchase Plan
Apply Now🔥 12 hours ago
Clinical Trial Manager overseeing clinical monitoring aspects of projects at CTI. Coordinating and managing clinical monitoring team operations and ensuring adherence to project standards.
🔥 14 hours ago
Senior Clinical Trial Manager overseeing site management for oncology clinical trials. Leading team direction from study initiation through closure while managing monitoring deliverables.
🇺🇸 United States – Remote
💵 $112k - $222k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 15 hours ago
Remote Study Design Lead translating sponsor protocol requirements into database design for clinical research projects. Collaborating with clients and internal teams throughout study design and development.
🇺🇸 United States – Remote
💵 $70k - $90k / year
💰 Post-IPO Debt on 2019-06
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 17 hours ago
Senior Clinical Trial Manager leading operational delivery of cell therapy clinical trials at Kyverna Therapeutics. Overseeing timelines, budget, quality, and cross-functional coordination for assigned studies.
🇺🇸 United States – Remote
💵 $155k - $180k / year
💰 $85M Series B on 2022-01
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🔥 17 hours ago
Assistant Clinical Study Manager supporting clinical trial operations at RTI International. Collaborating within a Data Coordinating Center to plan and execute clinical research projects effectively.