Clinical Project Manager
Clinical Trial Manager - Home based in Spain or Hybrid based in Barcelona
About this role
TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP) solutions.
The Clinical Trial Manager / Project Manager has the overall responsibility for managing projects in accordance with company policies, SOPs, regulatory requirements in addition to financial and contractual obligations
As part of our SRS/FSP team, you will be dedicated to one sponsor, a global biotech specialized in Oncology
Responsibilities
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Ensure that projects are delivered on-time, within scope and within budget and in compliance
with applicable quality standards
Manages the strategic aspects of projects, identify, analyze and minimize/mitigates any risk,
including the implications of difference technical and operational choices.
Communicates effectively with clients to successfully manage the relationship, identify needs
and evaluate alternative business solutions and strategies.
Develop and maintain Project Plans and timelines for their project and track progress
Ensure all study team members -are adequately trained on project specific systems and
procedures
Implements, and maintains sound business practices
Measure and evaluate project performance
Manage the project budget, profitability and ensure invoicing is performed on time and in
accordance with the scope of work
Working with the Finance & Accounting team to analyze profitability, revenue, margins and
utilization across their projects.
Manage the resource allocation, on the project, in collaboration with respective line managers
Facilitate internal and external communication
Report and escalate to management as needed
Establish and maintain relationship with third parties/vendors
Manages high-level deliverables across the organization
Participate in capability presentations/bid defenses, as needed.
Continually defines ways to increase customer satisfaction and deepen client relationships.
Contribute in review/develop procedures, guidelines, SOPs, metrics as needed
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Requirements
- Over 5 years of experience, preferably in early-stage oncology development and within small, dynamic biotechnology companies.
- Hands-on experience as a Clinical Research Associate (CRA) combined with study management experience.
- Strong background in clinical trial management, including vendor selection, study initiation, execution, monitoring, and closure of clinical studies.
- Proven experience in contingency planning and risk management during clinical trials.
- Preference for candidates with experience working in small, fast-paced biotech companies.
- Native Spanish speaker is required, with a good command of English.
- Flexibility to work remotely or in a hybrid model.
- Proactive, mature in clinical operations, and passionate about working in early-stage drug development in a fast-moving environment
Minimum Experience:
Technical Knowledge:
Risk Management:
Biotechnology Environment:
Language:
Work Model:
Personality Traits:
What we offer
We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You’ll be joining a team that values collaboration, innovation, and making a difference in the lives of patients
A Bit More About Us
Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.
Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.
- Department
- SRS South Europe
- Locations
- Barcelona
- Remote status
- Fully Remote
- Employment type
- Full-time
- REQ ID
- reqID235731
- Work Arragement
- Remote
Barcelona
Clinical Project Manager
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