Clinical Trial Oversight Manager

Amgen
Riyadh, منطقة الرياض
منذ أسبوعين

Saudi Arabia - Riyadh

JOB ID:
R-218102
ADDITIONAL LOCATIONS:
Saudi Arabia - Riyadh
WORK LOCATION TYPE:
Field Worker
DATE POSTED:
Jun. 16, 2025
CATEGORY:
Clinical
Responsibilities:
  • Primary point of contact for FSP vendor(s)
for resource and capacity management,
portfolio planning and prioritization,
performance management including the
identification, escalation and resolution of
quality and delivery issues
  • Provides support of clinical study execution
  • Provides GSO-SM functional area expertise
and actively collaborates in a dynamic crossfunctional
environment
  • Oversight of the site contracting, budgeting
and payment process
  • Line Manager of SCBAs

Key Activities:

  • Performs sponsor oversight activities of SM-FSP,
including staff performance (KPIs, report(s) metric
analysis/review), to ensure quality and delivery of Amgen
clinical trials.
  • Collaborates closely with SM-FSP Line Manager (FSPLM)
to ensure appropriate level of their staff oversight is
deployed.
  • Supports SM-FSP staff onboarding and training
  • Supervises staff involved in local site contracting and
budget management, insurance and payment process
  • Manages SCBA onboarding and training
  • Point of escalation for all stakeholders to support
resolution of issues eg quality, staff turnover and
performance concerns
  • Works with SM-FSP vendor(s) to ensure timely and
appropriate planning, resource and capacity management
from study start up to close-out
  • Conducts on-site quality visits with CRAs where/when
appropriate and supports the maintenance of Amgen
investigator site relationships
  • Supports inspection readiness, local country and site level
audits and regulatory inspections when applicable
including CAPA resolution
  • Organizes and leads the Functional Management Team
(FMT) Meetings and any other country-level project
review meetings, if applicable.
  • Involved in local and global site management and crossfunctional
stakeholder collaboration
  • Actively participates in role forums including local and
global functional and cross-functional initiatives.
Basic Qualifications:
  • Doctorate degree OR
  • Master’s degree OR
  • BA/BS/BSc or qualified nurse (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
  • Broad work experience working in life sciences or medically related
field, including clinical site management experience, obtained
working on clinical trials in a biotech, pharmaceutical or CRO
company
  • Experience as a CRA, CTA, and/or Clinical/Regional Manager in the
biopharmaceutical industry
  • Experience in a project leadership role
  • Experience working with or for Functional Service Provider or
Contract Research Organizations
  • Supervisory Experience
  • Knowledge of or work experience with a biopharmaceutical GRDCA
or QC department

Knowledge:

  • Familiarity with advanced concepts of clinical research
  • Extensive knowledge of ICH/GCP regulations and guidelines
  • Strong knowledge of clinical trial operations
  • Understanding of Functional Service Provider operational model
  • Computer and system operation skills
  • Relevant therapeutic area education and training
  • Detailed understanding of customer service
  • Demonstrated ability to anticipate and resolve problems.
Competencies:
  • Demonstrated ability to work independently with minimal supervision
  • Ability to work effectively in a team/matrix environment on multiple
projects
  • Excellence in relationship building
  • Ability to lead and influence in a positive manner
  • Leadership
  • Strong interpersonal skills
  • Excellent organizational and planning skills
  • Excellent oral and written communication
  • Language: Business English fluency
  • Attention to quality and detail
  • Ability to identify and resolve problems
  • Flexibility
  • Ability to write and present clearly using scientific and clinical issues
terminology
  • Attention to quality planning and execution
  • Ability for critical thinking and thinking out of the bo

تقديم
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