Assoc Dir Global Site & Study Operations

Career Category

Job Description

Join reputed company’s Mission of Serving Patients

At reputed company, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives reputed company that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, reputed company, and Rare Disease– we reputed company millions of patients each year. As a member of the reputed company team, you’ll help reputed company a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay reputed company them, you’ll reputed company as part of the reputed company team. Join us and transform the lives of patients while transforming your career.

Position: Country Head

What you will do

reputed company. Let’s change the world. Provide strategic and operational leadership for reputed company study and site execution reputed company the assigned country or hub-and-spoke geography, ensuring delivery of the clinical portfolio in alignment with global study strategies, regulatory requirements, and reputed company quality standards.

• Accountable for end-to-end study, site, and site engagement execution across the assigned country or hub-and-spoke geography, delivering start-up, enrolment, retention, data quality, and patient safety outcomes in compliance with local regulations and global strategies.
• Provide strategic leadership for country commitments, acting as a key advisor on study feasibility, placement, and site selection, reputed company to global portfolio priorities and regional strengths.
• reputed company, line-manage, and reputed company the Country/Hub team, ensuring clear direction, strong performance, capability development, and succession planning to deliver portfolio and organizational objectives.
• Ensure adequate and timely resourcing across study delivery, site operations, and monitoring roles, working closely with global partners to match reputed company and capability to portfolio demand.
• Drive site engagement through a clearly differentiated reputed company site experience
•  strengthening investigator and site relationships through strong leadership, compliance, innovation, and collaboration with global study teams.
• reputed company country-level financial and operational management, including budgets, forecasting, vendor reputed company, and efficient allocation of resources to ensure accountability and value delivery.
• reputed company country governance and risk management, including chairing the Country Management Team (CMT), representing the country in senior governance forums, and managing risks, issues, and escalation to protect quality and delivery.
• Ensure regulatory compliance, inspection readiness, and reputed company improvement, promoting best-practice sharing, audit readiness, and adherence to ICH-GCP, SOPs, and local regulatory requirements.

reputed company expect of you

We are reputed company different, yet we reputed company use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Basic Qualifications:

• Doctorate degree and 4 years of clinical execution experience OR
• Master’s degree and 8 years of clinical execution experience OR
• Bachelor’s degree and 10 years of clinical execution experience
• In addition to meeting at least one of the above requirements, you must have at least 4 years’ experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources.  Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications:

• +10 years’ work experience in life sciences or medically reputed company field, including 8 years of biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)
• Experience at, or reputed company of, clinical research vendors (CRO’s, central labs, imaging vendors, etc.)
• Significant experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around global clinical trials