Site Engagement Sr Mgr

Amgen Inc.

3.6

(9)

Riyadh, Saudi Arabia

Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging
  • #R-218104

    Position summary

    nd coherent voice as part of
    Amgen's overarching engagement strategy. Collaborate with other cross functional roles
    for 'tailored' global execution of study(ies).
    • Proactive and accountable to drive expansion of Amgen's strategic relationships and
    meet clinical operational needs as subject matter expert.
    • Primary site-facing, cross-study, operational decision-maker between Amgen and
    designated key sites for the purposes of establishing Amgen-Institutional operational
    working practices.
    • Maintain country expertise, site knowledge to navigate with Amgen and sites with
    targeted and tailored communication.
    • Develop, drive and monitor site operational strategies and performance across all
    therapeutic areas and studies, in strong collaboration with Amgen stakeholders.
    • Assimilate and report external feedback to evaluate and propose operational process
    efficiencies, focus and direction for site collaboration on clinical trials.
    • Orchestrate relationship management and strong internal alignment with Amgen
    stakeholders (medical, study management, site management, and other key -
    stakeholders) to drive operational efficiencies.
    • Strong collaboration with Regional and/or Local Trial Manager (RCTM/LTM*) to ensure
    clear roles and responsibilities. Communicate cross-study lessons learned and maintain
    consistent working relationships with sites.
    • Share information and cross-study KPIs to Key Stakeholders, e.g., DOM, DFM, CTOM,
    Study Managers etc.
    • Locally accountable for key, targeted sites execution of clinical studies
    • Build and develop strong relationships with key sites to engage with Amgen as Choice
    for clinical trial participation, to effectively advance site operational engagement and
    better understand current site processes to enhance our clinical trial execution.
    • Regular communication with key sites to connect on all trials/all stages to determine
    trends and opportunities and enhance site's experience with Amgen. On-site visits as
    appropriate (per site and situation).
    • Maintaining quick and direct access to key sites' leadership & operation teams, point of
    escalation for operational, cross-study potential barriers and operational issues.
    • Internal point of contact to navigate working with key sites, and to help key sites navigate
    working with Amgen.
    • Centralize and socialize site intelligence technology, such as working practices,
    operational documents, to enhance clinical trial efficiencies at site.
    • Participation in cross-functional task forces / process improvement groups.
    • GSO quality management
    • Actively participates in role forums including local and global functional and cross functional
    initiatives.
    • Participates in Functional Management Team (FMT) Meetings as required and applicable
    country-level project review meetings.

    Qualifications
    The knowledge and skills necessary to perform the duties of this position are
    typically acquired through the following combination of education, experience
    and knowledge, or the equivalent.
    Basic Qualifications
    • BA/BS/BSc or RN
    • 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)
    Preferred Qualifications
    • M.D., D.O., PhD, PharmD, Master's Degree
    • Country clinical operations experience and/or regional study management
    experience
    • Expertise and in-depth understanding of site engagement with clinical trials, or
    building and/or coordinating community research networks
    Knowledge
    • In depth understanding of drug development process, clinical trial conduct, ICH-GCP
    and local regulations, requirements, and guidelines
    • Project and Program management including oversight of quality, study deliverables,
    budgets and timelines
    • Various therapeutic area knowledge
    • Fluency in written and spoken English
    • Clinical trial management systems and reporting tools
    • Utilization of Key Performance Indicators (KPIs)

    Competencies
    • Commitment to uphold ethics and the Amgen values
    • Ability to work independently as well as in a team/matrix
    environment on multiple projects and countries
    • Analytical and problem solving skills
    • Decision making
    • Oral and written communication skills
    • Strategic operational planning and cross-functional
    leadership
    • Horizon scanning
    • Risk assessment and risk mitigation
    • Issue management and escalation
    • Project management
    • Organizational skills: planning, time management,
    prioritization, delegation
    • Teamwork, collaboration and relationship building skills
    across geographic areas, including: networking, negotiation
    and influencing skills across all levels with both
    internal/external stakeholders
    • Change management skills and learning ability
    • Patience, flexibility and high tolerance for ambiguity and
    change.

    .

    Why you should apply for a job to Amgen Inc.:

  • 67% say women are treated fairly and equally to men
  • 78% would recommend this company to other women
  • Ratings are based on anonymous reviews by Fairygodboss members.
  • Flexible work models that empower staff members to work where and when they are most productive
  • Award-winning PTO plan and bi-annual company-wide shutdowns
  • With 11 Employee Resource Groups, 60 chapters & 11000 members everyone has opportunity to connect, network & foster a culture of belonging