Associate Director, Clinical Trial Lead

What You'll Do Develop and oversee implementation of the study-level operational strategy for the successful delivery of clinical studies. Chair the Study Management Team (SMT) to drive development of scientifically robust, operationally feasible, and clear concepts/protocols.

Oversee delivery of studies by CROs to ensure quality execution in line with time and budget forecasts. Partner with the CRO SMT lead to ensure the CRO creates appropriate risk-mitigation plans and effectively identifies/resolves issues.

Establish and drive efficient team operations by establishing an open culture defined by communication, goal setting, and oversight of strategy implementation.

Ensure effective, consistent, efficient and compliant processes. Champion synergies among other studies, programs, and development units to enhance excellence in study planning and execution.

Who You Are Scientifically and clinically astute, you're a mission-driven individual with the strategic vision to see the big picture and assume responsibilities much broader and more meaningful than day-to-day operations.

Decisive, analytical and self-confident, you are determined to own all of your career and the difference you can make on the lives of others through your leadership and ability to inspire excellence.

Required Skills Bachelors Degree in a scientific discipline 8 + years in clinical operations management, overseeing outsourced clinical trials per quality, timeline, and budget expectations, preferably with a sponsor company and a CRO Related scientific and clinical expertise and exceptional project-management, risk-assessment, contingency-planning, and communication skill Extensive knowledge of clinical development related to one or more trial phases (I, II, III, or IV), as well as cross-functional drug development Unquestioned expertise in Good Clinical Practices (GCP), International Council for Harmonisation (ICH) guidelines and regulatory requirements for clinical development Ability to establish operational plans and support the CRO in executing them Effective CRO management skills and ability to adapt to the Global Clinical Operations (GCO) outsourcing model Preferred Skills Experience operationalizing nephrology clinical studies An advanced degree, such as a master's or Ph.

D in a related field Investigator site and/or monitoring experience Job Level: Management Additional Information The base compensation range for this role is: - Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.