Clinical Trials Manager I

Scorpion Therapeutics; California (MO); On-site; USD 90,000 - 130,000; Full time

Job summary

Cytokinetics is seeking a Clinical Trials Manager I to support its cardiovascular biopharma pipeline, focusing on Phase II/III operations, site management, and vendor oversight in South San Francisco.

You will coordinate study activities, ensure FDA/ICH-GCP compliance, manage CROs, and drive study start-up, conduct, and close-out with thorough documentation. Collaboration with finance and vendors and participation in study meetings will be essential.

Qualifications

• BA/BS in a science-related field.
• 1–3 years of clinical research experience, sponsor-side preferred.
• Strong communication, problem-solving, and organizational skills.
• Basic knowledge of FDA/ICH-GCP regulatory guidelines.
• Proficiency in MS Office applications.
• Willingness to travel ~20%.

Responsibilities

• Coordinate all study activities and ensure FDA/ICH-GCP compliance.
• Manage CROs and vendors; oversee study start-up, conduct, and close-out processes; maintain documentation quality.
• Collaborate with cross-functional teams including finance and vendors; participate in study meetings.

Skills

Regulatory knowledge

Study coordination

Vendor management

Cross-functional collaboration

Travel readiness

Education

BA/BS in science

Tools

MS Office

Job description

Role

Clinical Trials Manager I supporting Cytokinetics' cardiovascular biopharma pipeline, primarily focused on clinical operations for Phase II or III studies.

HighValue: supports cardiovascular drug development, Phase II/III, clinical operations, vendor management, regulatory compliance, documentation, sponsor experience preferred, on-site in South San Francisco with travel.

Responsibilities

• coordinate all study activities, ensure compliance with FDA and ICH-GCP guidelines, manage CROs and vendors, oversee study start-up, conduct, and close-out processes, and maintain documentation quality.
• Collaborate with cross-functional teams including finance and vendors, and participate in study meetings.

Qualifications

• BA/BS in a science-related field;
• 1-3 years of clinical research experience, preferably sponsor-side;
• strong communication, problem-solving, and organizational skills;
• basic knowledge of regulatory guidelines;
• proficiency in MS Office;
• willingness to travel (~20%).

Work Setup

onsite, approximately 20% travel.