Lead Study Manager, Clinical Trials

150 Altasciences Clinical Kansas Inc; Overland Park (KS); On-site; USD 95,000 - 130,000; Full time

Benefits offered by this job

Health/Dental/Vision

401(k)/RRSP with Employer Match

Paid Vacation and Holidays

Paid Sick and Bereavement Leave

Employee Assistance & Telehealth

Job summary

Altasciences is seeking a Study Manager to oversee the overall supervision, coordination and management of assigned clinical trials in compliance with GCP and SOPs. You will supervise study procedures, coordinate with Clinical Operations, and ensure audits and IP handling meet timelines and protocol requirements.

The role requires leadership, strong communication, and the ability to manage multiple trials in a fast-paced environment, with a focus on data integrity and participant confidentiality.

Qualifications

• High School diploma or GED required; college degree preferred.
• Excellent written and verbal communication (French and English in Montreal location).
• Customer service focused, able to work in a fast-paced environment.

Responsibilities

• Supervise and coordinate all study-related procedures in compliance with GCP and SOPs.
• Oversee trial progression and communicate with clients and internal teams.
• Coordinate staffing and staffing schedules to meet protocol needs.
• Ensure on-site file accuracy and readiness for audits.
• Record adverse events and manage study-related data per SOPs.

Skills

Leadership

Organizational skills

Communication

Bilingual English/French

Education

High School diploma or GED

College degree preferred

Job description

Altasciences is seeking a Study Manager to oversee the overall supervision, coordination and management of assigned clinical trials in compliance with GCP and SOPs. You will supervise study procedures, coordinate with Clinical Operations, and ensure audits and IP handling meet timelines and protocol requirements.

The role requires leadership, strong communication, and the ability to manage multiple trials in a fast-paced environment, with a focus on data integrity and participant confidentiality.