Clinical Trials Manager
hace 2 semanas
About the Role
We are seeking a highly motivated and organized individual to join our team as a Clinical Trials Manager in the Chronicity and Neurosciences area of knowledge. This is an exciting opportunity to work with a dynamic team, develop your skills, and contribute to the success of our clinical trials.
Job Summary
The successful candidate will be responsible for overseeing clinical trial activities, ensuring adherence to study protocols, Good Clinical Practice (GCPs), and regulatory requirements. You will also be involved in patient recruitment strategies, retention plans, monitoring compliance with study timelines, deliverables, and ethical guidelines, and resolving operational challenges that arise during the trial.
Main Responsibilities
- Clinical Trial Oversight and Coordination: Ensure all clinical trial activities adhere to the study protocol, GCPs, and regulatory requirements.
- Team Leadership and Mentorship: Mentor junior study coordinators, data entry staff, and other team members involved in clinical trials.
- Communication and Liaison: Work closely with principal investigators to ensure trials are conducted smoothly and effectively.
- Regulatory and Documentation Management: Ensure compliance with all applicable laws, regulations, and institutional policies.
- Study Planning and Logistics: Coordinate and schedule study visits, ensuring all pre-visit requirements are met.
- Quality Assurance: Verify all study data is accurate, complete, and entered into relevant systems promptly.
Required Skills and Qualifications
- Master's degree in Clinical Trials or a related field.
- More than 3 years of experience as a Study Coordinator.
- Knowledge of database programs.
- Ability to work independently as well as in a team environment.
- Good communication skills and fluency in written and spoken English.
Benefits
- Gross annual salary: €50,000 - €60,000.
- Full-time position: 40 hours/week.
- Starting date: Immediate.
- Contract: Linked to project (2 years approximately).
- Incorporation to Vall d'Hebron Research Institute (VHIR), a public sector institution.
- A scientific environment of excellence, highly dynamic, where high-end biomedical projects are continuously developed.
- Continuous learning and a wide range of responsibilities within a stimulating work environment.
- Individual training opportunities.
- Flexible working hours.
- 23 days of holidays + 9 personal days.
- Flexible Remuneration Program (including dining checks, health insurance, transportation, and more).
VHIR Embraces Equality and Diversity
We value diversity and promote equal opportunities in recruitment, hiring, training, and management for all staff within the organization, regardless of gender, civil status, family status, sexual orientation, gender identity and expression, religion, age, functional diversity, or ethnicity.
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