Manager, Clinical Trials

Scorpion Therapeutics; United States; Remote; USD 120,000 - 180,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Trials Manager to oversee all phases of complex studies, ensuring adherence to protocols, SOPs, and regulatory standards across remote U.S. sites.

You will lead vendor and CRO management, study start-up/close-out, budgeting, and cross-functional collaboration with data management and investigative sites to meet timelines, quality, and cost targets.

Qualifications

• Bachelor's in life sciences with 8+ years in clinical research, at least 4 years in a leadership role.
• Experience supporting CROs preferred.
• Knowledge of FDA regulations, ICH-GCP, and GxP standards essential.
• Strong skills in project management, vendor oversight, protocol development, and communication.
• Focus on early to late-phase trials, in a regulated setting, supporting biomarker or genomic testing in oncology or women's health.

Responsibilities

• Vendor and CRO management, study start-up and close-out, budgeting, monitoring study progress, and training staff.
• Collaboration with data management, investigative sites, and cross-functional teams to meet timelines, quality, and cost targets.

Skills

Project management

Vendor oversight

Protocol development

Communication

Education

Bachelor's in life sciences

Job description

Role

Clinical Trials Manager overseeing all phases of complex clinical studies, ensuring compliance with protocols, SOPs, and regulatory standards.

Responsibilities

• vendor and CRO management, study start-up and close-out, budgeting, monitoring study progress, and training staff.


• The role involves collaboration with data management, investigative sites, and cross-functional teams to meet timelines, quality, and cost targets.

Qualifications

• Bachelor's in life sciences with 8+ years in clinical research, at least 4 years in a leadership role managing clinical trials within regulated environments.


• Experience supporting CROs preferred.


• Knowledge of FDA regulations, ICH-GCP, and GxP standards essential.


• Skills include project management, vendor oversight, protocol development, and strong communication.

High-Value

• Focus on early to late-phase clinical trials, in a regulated setting, supporting biomarker or genomic testing in oncology or women's health.

Location

The position is remote within the USA, with no specified travel expectations.