Clinical Site Operations Lead (Study Management)

Logoslabs; San Francisco (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Logoslabs is seeking a Site Operations Manager I to oversee the on-time and on-budget delivery of clinical studies within a matrix environment. You will lead the study management team that plans, recruits, executes, and close-outs trials in accordance with SOPs, GCP/ICH, and FDA/state regulations.

In this role you will coordinate with internal and sponsor teams, manage resources and study finances, and ensure effective communication of progress, risks, and resolutions while maintaining

Qualifications

• Bachelor’s degree or equivalent applicable experience required.
• Minimum of 2+ years of pharmaceutical/biotech clinical study management experience.
• Medical and scientific knowledge preferred.

Responsibilities

• Develops a project management plan with cross-functional teams.
• Leads multi-disciplinary Study Management Team.
• End-to-end management of clinical studies within budget and timelines; plans resources and contingencies.
• Develops and monitors study metrics.
• Acts as primary client contact between Science 37 and sponsor project team.
• Manages study budgets, expenses and invoicing.

Skills

Study management

Budget and resources

Cross-functional leadership

Communication skills

Problem solving

Team leadership

Education

Bachelor’s degree or equivalent experience

Tools

MS Office

Google applications

Job description

Logoslabs is seeking a Site Operations Manager I to oversee the on-time and on-budget delivery of clinical studies within a matrix environment. You will lead the study management team that plans, recruits, executes, and close-outs trials in accordance with SOPs, GCP/ICH, and FDA/state regulations.

In this role you will coordinate with internal and sponsor teams, manage resources and study finances, and ensure effective communication of progress, risks, and resolutions while maintaining