Senior Clinical Lab Study Manager (Hybrid)

Pharmavise Corporation; Indianapolis (IN); Hybrid; USD 120,000 - 180,000; Full time

Benefits offered by this job

Health Insurance

Voluntary Benefits

401(k) Plan

Commuter Benefits

Paid Time Off (PTO)

Job summary

Pharmavise Corporation in Indianapolis, IN seeks a Senior Clinical Laboratory Associate — Pharmaceutical for a hybrid schedule. The role focuses on surge capacity delivery within CLS, serving as the single point of contact for study teams and CLS TPOs, managing data delivery, safety/biomarker studies, and study closeout.

Requires a Master’s or Ph.D. in Medical Science and 10–15+ years in project/program management, with pharma/diagnostics/CRO experience and strong communication and Excel skills.

Qualifications

• Master’s and/or Ph.D degree in the Medical Science field.
• 10-15+ years of experience in the Project/Program Management field.
• Prior experience in pharma, diagnostics or CRO environment.
• Experience in clinical research or a closely related field.
• Demonstrated ability to communicate clearly.
• Demonstrated attention to detail and organization.
• Skilled in excel for report combining and tracking.

Responsibilities

• Study level project management – including maintenance, data lock and closeout, document flow (review/approvals), budget management
• Single point of contact for study teams and CLS TPOs
• Tracking of safety, biomarker, PK and ADA samples as well as imaging and connected devices
• Query tracking and management
• Internal & External Engagement - Collaborate with internal business partners regarding CLS processes and business operations
• Collaborate with business partners and TPOs to ensure data delivery

Skills

Project management

Communication

Attention to detail

Excel

Education

Master’s and/or Ph.D in Medical Science

Job description

Pharmavise Corporation in Indianapolis, IN seeks a Senior Clinical Laboratory Associate — Pharmaceutical for a hybrid schedule. The role focuses on surge capacity delivery within CLS, serving as the single point of contact for study teams and CLS TPOs, managing data delivery, safety/biomarker studies, and study closeout.

Requires a Master’s or Ph.D. in Medical Science and 10–15+ years in project/program management, with pharma/diagnostics/CRO experience and strong communication and Excel skills.