We’re Hiring CLINICAL STUDY MANAGER – Clinical Operations Department
Are you an experienced clinical research professional ready to take the next step in your career? Join our Clinical Operations team at BCCC and play a pivotal role in leading, coordinating, and optimizing clinical studies that make a real impact on patients’ lives.
Location : Barcelona (Hybrid option available) Reports to : Head of Clinical Operations
About the Role
As a Clinical Study Manager, you’ll oversee the conduct and progress of clinical studies, ensuring the highest standards of quality, compliance, and operational excellence. You will guide and mentor Clinical Research Associates (CRAs), support project planning and execution, and collaborate closely with cross-functional teams to deliver successful outcomes.
This is a dynamic, hands‑on role that combines strategic oversight with operational leadership in a fast‑paced, collaborative environment.
Key Responsibilities
- Supervise and support the control and progress of ongoing clinical studies.
- Oversee CRA performance, ensuring compliance with GCP, regulatory requirements, and study protocols.
- Mentor and train CRAs, fostering professional growth and consistency across monitoring activities.
- Collaborate with the Project Manager (PM) in developing study‑specific documents such as the Monitoring Plan, Pharmacy Manual, and Laboratory Manual.
- Contribute to the design and implementation of risk‑based monitoring strategies.
- Participate in site communications and resolve complex issues in coordination with the PM.
- Review site feasibility questionnaires and qualification visit reports.
- Conduct quality control checks and support preparation of periodic study follow‑up reports.
- Engage in the preparation and presentation of Site Initiation Visit (SIV) materials.
- Provide training and mentorship to junior and trainee CRA profiles.
Required Qualifications
Degree in Medicine, Biology, Biochemistry, Pharmacy, Chemistry, or a related field.Postgraduate studies (Master’s or Advanced Course) in Clinical Research or equivalent demonstrated expertise.At least 4 years as a Senior CRA within the pharmaceutical or CRO industry, plus 1 year in a Clinical Study Manager or similar role.Strong understanding of GCP, clinical study regulatory frameworks, and data protection regulations.Proven experience with electronic systems such as eCRF, eCTMS, and eTMF.Familiarity with risk‑based monitoring principles.Advanced English level (spoken and written).Desirable : experience in clinical investigations with medical devices.Core Competencies & Skills
Excellent organization, prioritization, and independent work capabilities.Strong communication, negotiation, and leadership skills.Proactive, analytical, and solution‑oriented mindset.Rigorous attention to detail and adherence to quality standards.Proficient in cloud‑based IT tools and platforms.Comfortable working in multidisciplinary environments and managing complex timelines.Committed to continuous improvement and operational excellence.Working conditions
Full time positionOffices located in BarcelonaHybrid workCompetitive salaryExclusive employee discount club, giving you special benefits and discounts across a wide range of products and services.Starting date of the contract : November / December 2025Why Join Us?
At BCCC, we’re committed to advancing clinical research through innovation, collaboration, and scientific integrity. As part of our Clinical Operations team, you’ll work alongside passionate experts, manage impactful projects, and help deliver therapies that improve lives worldwide.
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