Clinical Laboratory Associate – Pharmaceutical

Jobtailor; Indianapolis (IN); On-site; USD 90,000 - 140,000; Part time

Job summary

Jobtailor in the United States is seeking an experienced Clinical Project Manager to oversee study-level activities, including maintenance, data lock, closeout, document flow reviews and budget oversight.

You will serve as the single point of contact for study teams and CLS TPOs, track safety, biomarkers, PK, ADA samples, imaging, and related queries, and collaborate with internal partners to ensure timely data delivery and adherence to CLS processes.

Qualifications

• Bachelor’s degree required.
• 6+ years of Clinical Industry experience.
• 3+ years of Clinical Research Assistant/Coordinator experience.
• 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.
• US-based contractor.

Responsibilities

• Perform study-level project management, including maintenance, data lock and closeout, document flow review and approvals, and budget management
• Serve as the single point of contact for study teams and CLS TPOs
• Track safety, biomarker, PK, and ADA samples, as well as imaging and connected devices
• Track and manage queries
• Collaborate with internal business partners regarding CLS processes and business operations
• Collaborate with business partners and TPOs to ensure data delivery
• Focus on specific tasks and deliverables during study maintenance and closeout
• Represent CLS to study teams and TPOs throughout study maintenance and closeout
• Not be trained on study startup activities

Skills

Clear Communication

Attention to Detail

Organizational Skills

Budget Management

Education

Bachelor’s degree

Tools

Excel

Job description

• Perform study-level project management, including maintenance, data lock and closeout, document flow review and approvals, and budget management
• Serve as the single point of contact for study teams and CLS TPOs
• Track safety, biomarker, PK, and ADA samples, as well as imaging and connected devices
• Track and manage queries
• Collaborate with internal business partners regarding CLS processes and business operations
• Collaborate with business partners and TPOs to ensure data delivery
• Focus on specific tasks and deliverables during study maintenance and closeout
• Represent CLS to study teams and TPOs throughout study maintenance and closeout
• Not be trained on study startup activities

Requirements

• Bachelor’s degree required
• 6+ years of Clinical Industry experience
• 3+ years of Clinical Research Assistant/Coordinator experience
• 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
• US-based contractor

Core Competencies

Demonstrates expertise in clinical project management, including data lock, closeout processes, and budget management. Proficient in collaborating with study teams and business partners to ensure timely data delivery and adherence to CLS processes.

Highest-signal resume keywords

• Clinical Project Management
• Clinical Research Experience
• Budget Management
• Excel Proficiency
• Attention to Detail

Hard Skills

• Clinical Research
• Data Lock
• Closeout Processes
• Budget Management
• Query Management

Soft Skills

• Clear Communication
• Organizational Skills

Industry Keywords

• Clinical Industry
• Pharma
• Diagnostics
• CRO Environment
• Clinical Research Assistant

Tools & Technologies

• Excel