Position:
Clinical Study Coordinator
Location:
Madrid - onsite
Employment type:
TEMPORARY
Experience:
Minimum 3 years managing clinical trial units, preferably in Phase I.
OverviewWe are seeking a Clinical Trial Coordinator with proven experience in managing Phase I trials to join our team in Barcelona. The individual will coordinate, supervise, and ensure proper execution of clinical trials, maintaining compliance with regulatory standards, study protocols, and quality standards.
Responsibilities
Plan, coordinate, and supervise all activities related to Phase I clinical trials.
Manage the selection, training, and supervision of trial personnel.
Ensure compliance with study protocols, EMA, FDA, ICH-GCP regulations, and internal policies.
Coordinate preparation and review of clinical documentation, reports, and records.
Oversee documentation management, including informed consent forms and adverse event reports.
Collaborate with investigators, sponsors, and stakeholders for proper study execution.
Monitor study progress and resolve potential issues.
Participate in regulatory audits and inspections.
Stay updated on regulations and advancements in Phase I trials.
Requirements
Bachelor's degree in Health Sciences, Pharmacy, Biomedicine, or related field.
At least 3 years of experience managing clinical trial units, preferably in Phase I.
Deep knowledge of GCP and related regulations.
Experience in hospital or specialized clinical trial units.
Strong organizational, leadership, and communication skills.
Ability to work in a dynamic, multidisciplinary environment.
Fluent in English and Spanish, spoken and written.
Benefits
Join an innovative, growing team with professional development opportunities.
Collaborative work environment in Barcelona.
Competitive salary and additional benefits.
Selection ProcessExpect contact via phone or email. The process may include in-person or virtual interviews, possibly with a test. We aim to keep candidates informed throughout.
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