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Assoc Dir Global Site & Study Operations

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Assoc Dir Global Site & Study Operations

Turkiye - Istanbul Apply Now
JOB ID: R-236943 ADDITIONAL LOCATIONS: Turkiye - Istanbul WORK LOCATION TYPE: Remote DATE POSTED: Feb. 18, 2026 CATEGORY: Clinical Development

Accountabilities

The Country Study and Site Operations Head is accountable to drive all country and hub & spoke execution and quality measures, including study operations, site operations, and site engagement, while ensuring operational capabilities support the delivery of the geographic portfolio with high-quality data in compliance with local regulations.

Ensure study execution aligns with global strategies across trials and act as a key advisor for country commitments.

Provide leadership and line management to the Country/Hub team, offering clear guidance, fostering capability development, and driving portfolio objectives.

Represent the country strategically in organizational initiatives at all levels.

Lead the Country Management Team (CMT).

. Ensure Adequate resourcing

Responsibilities

Accountable for all study execution in assigned geography and quality metrics including delivering study start-up, patient enrollment, retention trends, and data flow metrics in alignment with global strategies across trials, serving as key advisor for country commitments

Oversee clinical study budgets and forecasting to ensure efficient use of resources and financial accountability.

Build, lead, and develop the Country/Hub team to effectively manage resources, ensuring appropriately skilled and high-performing staff to deliver the portfolio and meet organizational deliverables.

Drive country site engagement by leading SEL AD and/or SELs, aligning with global strategy, ensuring compliance, strengthening partnerships, and securing Partner-of-Choice positioning through innovation and leadership collaboration.”

Shape and foster collaboration between local functional teams and global study teams to drive delivery of study portfolio in assigned geography

Partner with internal stakeholders to monitor study progress and drive local actions plan & issue resolution, and aggregates country progress and challenges for senior management

Represent country in governance meetings, communicating cross-study progress to region / CPSO

Advocate for study placement in considerations of strengths and growth opportunities of assigned geography

Lead internal and external meetings to ensure delivery on portfolio targets

Key advisor for site selection, and identifies & communicates priority sites, allocating resources as required

Point of escalation to support resolution of country-wide issues including risks which impact delivery or quality of clinical trials and/ patient safety

Lead country-level risk assessments and implement mitigation strategies to ensure patient safety, compliance, and trial continuity

Oversees vendor selection, setup, performance oversight across local roles (study delivery, monitoring) in alignment with budget considerations and serves as point-of-escalation

Promote continuous improvement and best practice sharing to enhance operational efficiency and site engagement.

Build and develop strong local leadership and study teams to deliver on portfolio goals and support long-term organizational capability

Ensures adherence to key requirements (e.g., ICH-GCP, SOP, country regulations), study inspection readiness, internal audits and CAPA processes

Work with SDRM to ensure timely and adequately resourcing for all roles

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