Associate Director Clinical Operations

About the role

A leading Pharmaceutical Company located in MA is hiring an Associate Director Clinical Operations with 5+ years of industry experience. If you want to be a part of this groundbreaking work, please apply!

Responsibilities

• Provide leadership and guidance to clinical trial teams supporting innovative advanced therapy clinical trials.
• Collaborate with internal cross-functional teams, clinical sites, and CRO partners to execute global clinical programs in a safe, ethical, and compliant manner.
• Ensure trials adhere to ICH GCP, federal, international, and local regulatory requirements.
• Manage and forecast trial budgets and timelines, ensuring alignment with company objectives.
• Partner with US, EU, and international colleagues, CROs, and investigators to identify risks and develop effective trial plans.
• Develop high-quality study deliverables such as Protocols, CRFs, SAPs, CSRs, and manuals.
• Evaluate KPIs, KRIs, and SOPs; identify gaps and propose solutions for compliance and efficiency.
• Contribute to regulatory filings domestically and internationally.
• Mentor and develop Clinical Operations team members, participating in staffing, performance management, and talent development.
• Interact regularly with senior management on project and departmental initiatives.
• May oversee a team to achieve organizational goals.

Requirements

• Bachelor’s Degree in Life Sciences or related field
• 10+ years of progressive experience in clinical operations, with at least 5 years in a biopharmaceutical organization
• Experience overseeing CRO selection, contracting, and management
• Thorough understanding of GCP and ICH regulations, clinical trial monitoring, and compliance
• Prior experience in advanced therapies clinical research is desirable
• Strong written and verbal communication skills
• Ability to work cross-departmentally and cross-functionally
• Competent in data management, interpretation, and communication
• Excellent interpersonal, conflict resolution, decision-making, and delegation skills
• Occasional travel (up to 5%)

Qualifications

• Experience in managing clinical trials from start-up to closeout
• Knowledge of regulatory guidelines and compliance standards
• Strong project management and budgeting skills
• Effective communication and collaboration abilities

Skills

• Strong leadership and mentoring skills
• Expertise in clinical trial processes and procedures
• Proficiency in data analysis and reporting
• Ability to manage multiple projects simultaneously

Benefits

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

Pay

The salary range for this position is $135,000.00 - $170,000.00.

Schedule

The work model is Hybrid – onsite 2 days per week.