Study Oversight Manager

**Career Category** ------------------- Clinical Development **Job Description** ------------------- Accountabilities • The Study Oversight Manager (SOM) is responsible for leading and managing the resourcing, collaboration, and performance of FSP suppliers at the country level. • Acts as the main contact and escalation point for FSP suppliers, working cross-functionally to support clinical study execution and ensure efficient, high-quality clinical trial results. • Works together with LSOMs to oversee key country-level suppliers involved in study delivery. Responsibilities • Act as the main liaison for FSP supplier(s) regarding resource and capacity management, portfolio planning, and prioritization throughout the study lifecycle from startup to close-out. • Facilitate onboarding and training for FSP roles, including CRAs and CTAs. • Monitor supplier performance by tracking metrics and ensuring the overall quality of work delivered by FSP staff. • Identify, escalate, and resolve issues related to quality and delivery. • Work closely with LSOMs to provide appropriate staff oversight and uphold quality standards across Amgen clinical trials, including occasional on-site quality visits. • Promote effective collaboration between CRA and CTA roles and other country-specific positions to maintain consistent communication with sites and alignment with global strategies. • Collect and communicate country-wide concerns by consolidating feedback from FSPs, offering senior management an aggregated view of FSP trends and challenges. • Manage and oversee FSP supplier performance in relation to study milestones and quality objectives. • Support inspection readiness, including local country and site-level audits, as well as regulatory inspections when necessary. • Assist in maintaining relationships with Amgen investigators within the country. • Participate in cross-functional task forces and process improvement initiatives. Qualifications Describe the knowledge and skills necessary to perform the duties of this role. Include a  combination of education, experience, knowledge, or the equivalent Minimum Requirements • Doctorate degree OR • Master’s degree and 2 years of clinical execution experience OR • Bachelor’s degree and 4 years of clinical execution experience • Associate’s degree and 8 years of clinical execution experience OR  • High school diploma / GED and 10 years of clinical execution experience " • Work experience in life sciences or medically related field, including biopharmaceutical  clinical research experience (clinical research obtained working on clinical trials in a biotech,  pharmaceutical or CRO company, or other relevant clinical setting) • In addition to meeting at least one of the above requirements, you must have 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 Requirements (based off CTOM) • 5 years’ work experience in life sciences or medically related field, including 3 years of  biopharmaceutical clinical research experience obtained working on clinical trials in a  biotech, pharmaceutical or CRO company • Experience at, or oversight of, clinical research suppliers (CRO’s, central labs, imaging  suppliers, etc.)Experience as a CRA, CTA, and/or Clinical/Regional Manager in the  biopharmaceutical industry • Experience managing and supervising clinical trial staff across multiple studies" Competencies • Demonstrates expertise in identifying site-level challenges, applying data-driven strategies,  and implementing corrective actions to optimize trial performance • Experience supporting change management initiatives, including updating of documentation  and processes • Skilled in planning and implementation of country level operational plan, enhancing  compliance, and driving continuous improvement initiatives for efficient and effective study  execution • Ability to recognize, highlight and resolve issues. Demonstrates curiosity and willingness to take  on new tasks. • Ability to support processes around site preparedness and smooth trial execution across all  study phases and end-to-end activities  • Experience with overseeing suppliers • Commitment to quality trial execution, risk identification and risk management, and audit  readiness  • Open-mindedness towards skill development and active participation in internal training to  build knowledge of clinical trial processes. • Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools. Ability to maintain  accurate and timely data entry. Skilled in managing clinical trial data flow, investigator  documentation, and protocol adherence while ensuring regulatory compliance • Understands importance of accuracy in documentation, data tracking, and compliance  checks. Identifies discrepancies and escalates appropriately. • Understanding of the clinical and pharmaceutical drug development process and clinical trial  execution principles  For union related matters, please contact: [email protected] . **Salary Range** 684,476.10 SEK - 926,055.90 SEK