Clinical Trial Manager

Scorpion Therapeutics; United States; On-site; USD 115,000 - 200,000; Full time

Benefits offered by this job

Annual bonus

Equity

Comprehensive benefits

Job summary

Scorpion Therapeutics is seeking an experienced Clinical Trial Manager to lead global Phase 2 studies, coordinate CROs, sites, and internal teams to ensure timely delivery and data integrity.

You will plan study timelines, manage enrollment, monitor safety, and ensure compliance with ICH-GCP, HIPAA, and regulatory requirements. The role requires a BS in Life Sciences and 3–5+ years in CTM roles, with strong leadership and communication in a fast-paced biotech environment.

Qualifications

• BS in Life Sciences; 3+ years (CTM) / 5+ years (Sr. CTM) as a project/clinical trial manager in biotech/pharma.
• Experience on large, global, complex Phase 2 clinical trials.
• Knowledge of regulatory and ICH GCP guidelines, HIPAA, and Protection of Human Research Subjects.
• Strong project management (manage multiple trials).
• Excellent problem‑solving, leadership, and communication skills.
• Ability to work in a fast‑paced, cross‑functional environment.

Responsibilities

• Contribute to planning, implementation, and execution of a global clinical trial
• Manage vendors to support clinical trial execution
• Plan, execute, and lead study-specific meetings (e.g., internal core team, investigator meetings)
• Provide input to design Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.
• Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites, and contract personnel
• Manage study timelines and metrics to ensure completion of deliverables
• Support site selection, qualification, initiation, and monitoring activities
• Review monitoring reports and resolve site-related issues
• Ensure timely enrollment and data collection
• Collaborate with data management to ensure data integrity and timely database lock
• Review/analyze clinical trial data to identify trends and potential issues
• Track/review protocol deviations and assess impact
• Develop relationships with investigators and site staff
• Coordinate with CRO and Medical Monitor to summarize safety/efficacy data
• Partner with translational medicine on bioanalytical sampling plan incorporation and outputs
• Maintain accurate and complete trial documentation
• Proactively identify and resolve clinical project issues

Skills

Project management

Leadership

Communication

Cross-functional collaboration

Problem solving

Education

BS in Life Sciences

Job description

How you’ll make an impact:

• Contribute to planning, implementation, and execution of a global clinical trial


• Manage vendors to support clinical trial execution


• Plan, execute, and lead study-specific meetings (e.g., internal core team, investigator meetings)


• Provide input to design Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.


• Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites, and contract personnel


• Manage study timelines and metrics to ensure completion of deliverables


• Support site selection, qualification, initiation, and monitoring activities


• Review monitoring reports and resolve site-related issues


• Ensure timely enrollment and data collection


• Collaborate with data management to ensure data integrity and timely database lock


• Review/analyze clinical trial data to identify trends and potential issues


• Track/review protocol deviations and assess impact


• Develop relationships with investigators and site staff


• Coordinate with CRO and Medical Monitor to summarize safety/efficacy data


• Partner with translational medicine on bioanalytical sampling plan incorporation and outputs


• Maintain accurate and complete trial documentation


• Proactively identify and resolve clinical project issues

Skills and experience you’ll bring:

• BS in Life Sciences; 3+ years (CTM) / 5+ years (Sr. CTM) as a project/clinical trial manager in biotech/pharma


• Experience on large, global, complex Phase 2 clinical trials


• Knowledge of regulatory and ICH GCP guidelines, HIPAA, and Protection of Human Research Subjects


• Strong project management (manage multiple trials)


• Excellent problem‑solving, leadership, and communication skills


• Ability to work in a fast‑paced, cross‑functional environment

Compensation:

• Anticipated base salary: $115,000–$200,000; eligibility for annual bonus, equity, and comprehensive benefits