Requirements: English
Company: Oxford Global Resources
Region: Vitoria-Gasteiz , Basque Country
Clinical Trial Manager (CTM) Oncology Biotech Project
Location:
Remote / Europe-based (with occasional travel) Contract Type:
Permanent direct with Biotech Company Start Date:
Immediate or asap
Oxford Global Resources
is seeking a
highly motivated Clinical Trial Manager (CTM)
to join a
cutting-edge global biotech company
focused on developing a diverse pipeline of
precision oncology therapeutics
targeting the
Tumor Microenvironment (TME) . The position offers the opportunity to be part of a
first-in-human clinical program , with studies launching in
Spain and the U.S. This is a unique opportunity to contribute to the
early-stage clinical development
of innovative cancer therapies, working closely with senior leadership and external partners.
Key Responsibilities Report directly to the
Chief Medical Officer (CMO)
and lead the
operational execution
of clinical activities. Oversee
first-in-human (FIH)
oncology trials in Spain and the U.S., with
externalized CRO oversight . Ensure
GCP and ICH E6(R2)
compliance across all clinical activities. Monitor trial progress, recruitment metrics, site performance, and
CRO deliverables . Supervise
sample tracking ,
eCRF data entry , and
site-level documentation . Coordinate with central laboratories, vendors, and investigators for clinical logistics and drug supply. Participate in the preparation and review of key trial documents:
protocols ,
ICFs ,
trial manuals ,
patient materials , etc. Evaluate metrics and create
corrective action plans
to address deviations. Ensure timely documentation and adherence to
regulatory requirements
(EMA/FDA). Prepare and monitor
trial budgets , vendor contracts, and operational timelines. Represent the company in
investigator meetings , study team meetings, and site communications.
Requirements Bachelors degree in
Life Sciences, Healthcare, or Business Management . Proven experience as a
Clinical Trial Manager , ideally in
oncology
or early-phase trials. Strong knowledge of
GCP, ICH, FDA/EMA regulations , and clinical trial logistics. Previous experience
managing CROs, sites, vendors , and cross-functional teams. Excellent
communication, leadership , and
problem-solving
skills. Highly organized,
results-driven , and adaptable to dynamic environments. Experience with
clinical trial documentation systems
and eCRFs.
Why Join?
Be part of a
transformational oncology program
from early clinical development. Contribute to
cutting-edge precision medicine
in a fast-moving, innovative biotech. Collaborate closely with
executive leadership , playing a
strategic and hands-on role . Engage in a
high-impact, mission-driven environment
with global scope.
Interested?
Apply now or contact Oxford Global Resources to learn more about this opportunity and how to join a biotech team redefining cancer treatment.
Desired Skills and Experience #clinicalresearchjobs #clinicaltrialsjobs #projectmanagementjob